Related gene-specific medical variations for Gene (Select 28992) - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3056264	NM_013280.5(FLRT1):c.933C>T (p.Arg311=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	FLRT1-related condition	GLikely benign
Select item 3047412	NM_013280.5(FLRT1):c.951G>A (p.Leu317=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	FLRT1-related condition	GLikely benign
Select item 2641907	NM_013280.5(FLRT1):c.1029G>A (p.Val343=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2634534	NM_013280.5(FLRT1):c.1394G>A (p.Arg465Gln)	FLRT1, MACROD1 (R437Q +1 more)	Single nucleotide variant (missense variant +1 more)	FLRT1-related condition	GUncertain significance
Select item 2609285	NM_013280.5(FLRT1):c.1027G>C (p.Val343Leu)	FLRT1, MACROD1 (V343L +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2595718	NM_013280.5(FLRT1):c.1340C>T (p.Thr447Met)	FLRT1, MACROD1 (T419M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2592906	NM_013280.5(FLRT1):c.1705G>A (p.Val569Ile)	FLRT1, MACROD1 (V541I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2589632	NM_013280.5(FLRT1):c.1882C>T (p.Arg628Cys)	FLRT1, MACROD1 (R600C +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2588206	NM_013280.5(FLRT1):c.1211C>T (p.Thr404Met)	FLRT1, MACROD1 (T376M +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2557624	NM_013280.5(FLRT1):c.1288A>G (p.Met430Val)	FLRT1, MACROD1 (M430V)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2491115	NM_013280.5(FLRT1):c.32C>A (p.Thr11Asn)	MACROD1, FLRT1 (T11N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2401831	NM_013280.5(FLRT1):c.1672G>A (p.Gly558Ser)	MACROD1, FLRT1 (G558S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2397586	NM_013280.5(FLRT1):c.187G>A (p.Gly63Ser)	FLRT1, MACROD1 (G63S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2389867	NM_013280.5(FLRT1):c.1168G>A (p.Ala390Thr)	MACROD1, FLRT1 (A390T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2326771	NM_013280.5(FLRT1):c.542T>G (p.Leu181Arg)	FLRT1, MACROD1 (L181R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2324778	NM_013280.5(FLRT1):c.1360A>C (p.Thr454Pro)	MACROD1, FLRT1 (T454P)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2312285	NM_013280.5(FLRT1):c.1811G>A (p.Gly604Glu)	MACROD1, FLRT1 (G604E)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2292649	NM_013280.5(FLRT1):c.1119C>A (p.Ser373Arg)	FLRT1, MACROD1 (S373R)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2291761	NM_013280.5(FLRT1):c.676C>T (p.Arg226Cys)	FLRT1, MACROD1 (R226C)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2262614	NM_013280.5(FLRT1):c.1295C>T (p.Thr432Met)	MACROD1, FLRT1 (T432M)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2256786	NM_013280.5(FLRT1):c.1737G>C (p.Gln579His)	FLRT1, MACROD1 (Q579H)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2252111	NM_013280.5(FLRT1):c.1796A>G (p.Asp599Gly)	FLRT1, MACROD1 (D599G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2248361	NM_013280.5(FLRT1):c.1798T>A (p.Tyr600Asn)	FLRT1, MACROD1 (Y600N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2229577	NM_013280.5(FLRT1):c.1846G>A (p.Gly616Ser)	FLRT1, MACROD1 (G616S)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2226068	NM_013280.5(FLRT1):c.514G>A (p.Ala172Thr)	FLRT1, MACROD1 (A172T)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 1651466	NM_013280.5(FLRT1):c.1389T>C (p.Ser463=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1635114	NM_013280.5(FLRT1):c.825C>T (p.Leu275=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1616138	NM_013280.5(FLRT1):c.123C>T (p.Leu41=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1563980	NM_013280.5(FLRT1):c.186C>T (p.Asn62=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1446859	NM_013280.5(FLRT1):c.866C>T (p.Thr289Met)	FLRT1, MACROD1 (T289M)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1417202	NM_013280.5(FLRT1):c.1158C>T (p.Gly386=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1402858	NM_013280.5(FLRT1):c.290G>C (p.Gly97Ala)	FLRT1, MACROD1 (G97A)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1374536	NM_013280.5(FLRT1):c.1733A>G (p.His578Arg)	FLRT1, MACROD1 (H578R)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1348453	NM_013280.5(FLRT1):c.1042G>A (p.Ala348Thr)	FLRT1, MACROD1 (A348T)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1170621	NM_013280.5(FLRT1):c.1878G>A (p.Pro626=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy +1 more	GBenign/Likely benign
Select item 1170348	NM_013280.5(FLRT1):c.1548C>T (p.Tyr516=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1169624	NM_013280.5(FLRT1):c.1170G>T (p.Ala390=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1167057	NM_013280.5(FLRT1):c.1965C>T (p.Tyr655=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1167056	NM_013280.5(FLRT1):c.1566C>T (p.Pro522=)	FLRT1, MACROD1	Single nucleotide variant (intron variant +1 more)	Peripheral neuropathy	GBenign
Select item 1167055	NM_013280.5(FLRT1):c.288C>T (p.Ala96=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1166778	NM_013280.5(FLRT1):c.1893A>G (p.Glu631=)	FLRT1, MACROD1	Single nucleotide variant (intron variant +1 more)	Peripheral neuropathy	GBenign
Select item 1166605	NM_013280.5(FLRT1):c.57G>A (p.Thr19=)	MACROD1, FLRT1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1165249	NM_013280.5(FLRT1):c.735C>T (p.Ser245=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1165132	NM_013280.5(FLRT1):c.714C>T (p.Arg238=)	MACROD1, FLRT1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GBenign
Select item 1165131	NM_013280.5(FLRT1):c.246T>C (p.Asp82=)	FLRT1, MACROD1	Single nucleotide variant (intron variant +1 more)	Peripheral neuropathy	GBenign
Select item 1156519	NM_013280.5(FLRT1):c.1719C>T (p.Ile573=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1153896	NM_013280.5(FLRT1):c.1919C>A (p.Pro640His)	FLRT1, MACROD1 (P640H)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1152880	NM_013280.5(FLRT1):c.1482G>C (p.Leu494=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1151623	NM_013280.5(FLRT1):c.495C>T (p.Thr165=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1150098	NM_013280.5(FLRT1):c.996T>C (p.Cys332=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1147569	NM_013280.5(FLRT1):c.1428C>T (p.Ala476=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1147502	NM_013280.5(FLRT1):c.1287C>T (p.Pro429=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1137368	NM_013280.5(FLRT1):c.1443G>A (p.Thr481=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1136645	NM_013280.5(FLRT1):c.1629G>A (p.Gln543=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1135668	NM_013280.5(FLRT1):c.1926C>T (p.Asn642=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1131761	NM_013280.5(FLRT1):c.762G>A (p.Ser254=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1128795	NM_013280.5(FLRT1):c.285C>T (p.Asn95=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1127499	NM_013280.5(FLRT1):c.342C>T (p.Tyr114=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1126543	NM_013280.5(FLRT1):c.1326C>T (p.His442=)	FLRT1, MACROD1	Single nucleotide variant (intron variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1119373	NM_013280.5(FLRT1):c.94C>A (p.Arg32=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1115139	NM_013280.5(FLRT1):c.585G>C (p.Gly195=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1114417	NM_013280.5(FLRT1):c.2001C>T (p.Pro667=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1112150	NM_013280.5(FLRT1):c.1799A>G (p.Tyr600Cys)	FLRT1, MACROD1 (Y600C)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1110522	NM_013280.5(FLRT1):c.1362G>A (p.Thr454=)	MACROD1, FLRT1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1109864	NM_013280.5(FLRT1):c.723C>T (p.Asp241=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1107240	NM_013280.5(FLRT1):c.228C>T (p.Pro76=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1105924	NM_013280.5(FLRT1):c.945C>T (p.Asp315=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1101046	NM_013280.5(FLRT1):c.699G>A (p.Leu233=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1095307	NM_013280.5(FLRT1):c.1155C>T (p.Gly385=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1092352	NM_013280.5(FLRT1):c.180C>T (p.Cys60=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1086391	NM_013280.5(FLRT1):c.777G>A (p.Ser259=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 1085735	NM_013280.5(FLRT1):c.1122G>C (p.Glu374Asp)	FLRT1, MACROD1 (E374D)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy +1 more	GLikely benign
Select item 1061128	NM_013280.5(FLRT1):c.1277T>C (p.Ile426Thr)	FLRT1, MACROD1 (I426T)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy +1 more	GUncertain significance
Select item 1055905	NM_013280.5(FLRT1):c.86T>A (p.Met29Lys)	FLRT1, MACROD1 (M29K)	Single nucleotide variant (intron variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1054375	NM_013280.5(FLRT1):c.1202C>A (p.Ser401Tyr)	FLRT1, MACROD1 (S401Y)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1043451	NM_013280.5(FLRT1):c.677G>A (p.Arg226His)	MACROD1, FLRT1 (R226H)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1025289	NM_013280.5(FLRT1):c.1665C>T (p.Gly555=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1025266	NM_013280.5(FLRT1):c.915C>A (p.Asn305Lys)	FLRT1, MACROD1 (N305K)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy +1 more	GUncertain significance
Select item 1016606	NM_013280.5(FLRT1):c.1976G>A (p.Arg659Gln)	FLRT1, MACROD1 (R659Q)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1015495	NM_013280.5(FLRT1):c.176G>A (p.Arg59His)	FLRT1, MACROD1 (R59H)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1009229	NM_013280.5(FLRT1):c.1229T>A (p.Phe410Tyr)	MACROD1, FLRT1 (F410Y)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1008089	NM_013280.5(FLRT1):c.881G>T (p.Arg294Leu)	FLRT1, MACROD1 (R294L)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1003977	NM_013280.5(FLRT1):c.2006T>C (p.Ile669Thr)	FLRT1, MACROD1 (I669T)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 1002428	NM_013280.5(FLRT1):c.389G>A (p.Arg130Gln)	FLRT1, MACROD1 (R130Q)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 969374	NM_013280.5(FLRT1):c.443C>G (p.Ala148Gly)	FLRT1, MACROD1 (A148G)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 958559	NM_013280.5(FLRT1):c.1936C>T (p.Leu646Phe)	MACROD1, FLRT1 (L646F)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 957887	NM_013280.5(FLRT1):c.581C>T (p.Ser194Leu)	FLRT1, MACROD1 (S194L)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy +1 more	GUncertain significance
Select item 954974	NM_013280.5(FLRT1):c.1993G>A (p.Gly665Ser)	FLRT1, MACROD1 (G665S)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 951943	NM_013280.5(FLRT1):c.496G>A (p.Val166Ile)	FLRT1, MACROD1 (V166I)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 948270	NM_013280.5(FLRT1):c.445C>T (p.Arg149Cys)	FLRT1, MACROD1 (R149C)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 941259	NM_013280.5(FLRT1):c.1757G>A (p.Arg586Gln)	FLRT1, MACROD1 (R586Q)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 859555	NM_013280.5(FLRT1):c.977G>A (p.Arg326Lys)	FLRT1, MACROD1 (R326K)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 857225	NM_013280.5(FLRT1):c.251C>T (p.Thr84Ile)	FLRT1, MACROD1 (T84I)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 845837	NM_013280.5(FLRT1):c.1775G>A (p.Arg592Gln)	FLRT1, MACROD1 (R592Q)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 842634	NM_013280.5(FLRT1):c.471C>A (p.His157Gln)	FLRT1, MACROD1 (H157Q)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 840095	NM_013280.5(FLRT1):c.1792G>A (p.Asp598Asn)	FLRT1, MACROD1 (D598N)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases +1 more	GUncertain significance
Select item 835656	NM_013280.5(FLRT1):c.1646C>T (p.Ala549Val)	FLRT1, MACROD1 (A549V)	Single nucleotide variant (missense variant +1 more)	Peripheral neuropathy	GUncertain significance
Select item 782187	NM_013280.5(FLRT1):c.36C>T (p.Thr12=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 772484	NM_013280.5(FLRT1):c.1212G>A (p.Thr404=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign
Select item 706652	NM_013280.5(FLRT1):c.1653G>A (p.Leu551=)	FLRT1, MACROD1	Single nucleotide variant (synonymous variant +1 more)	Peripheral neuropathy	GLikely benign

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