Related gene-specific medical variations for Gene (Select 84182) - ClinVar

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Items: 61

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3126633	NM_032222.3(MINDY4):c.929C>G (p.Ser310Cys)	INMT-MINDY4, MINDY4 (S310C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126632	NM_032222.3(MINDY4):c.818G>A (p.Gly273Asp)	INMT-MINDY4, MINDY4 (G273D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126631	NM_032222.3(MINDY4):c.787A>G (p.Ser263Gly)	INMT-MINDY4, MINDY4 (S263G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126630	NM_032222.3(MINDY4):c.785C>G (p.Ser262Trp)	INMT-MINDY4, MINDY4 (S262W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126629	NM_032222.3(MINDY4):c.752T>G (p.Leu251Arg)	INMT-MINDY4, MINDY4 (L251R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126628	NM_032222.3(MINDY4):c.752T>C (p.Leu251Pro)	INMT-MINDY4, MINDY4 (L251P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126627	NM_032222.3(MINDY4):c.742G>A (p.Val248Ile)	INMT-MINDY4, MINDY4 (V248I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126626	NM_032222.3(MINDY4):c.691C>T (p.Arg231Trp)	INMT-MINDY4, MINDY4 (R231W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126625	NM_032222.3(MINDY4):c.686T>C (p.Leu229Pro)	INMT-MINDY4, MINDY4 (L229P)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126624	NM_032222.3(MINDY4):c.682T>C (p.Tyr228His)	INMT-MINDY4, MINDY4 (Y228H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126623	NM_032222.3(MINDY4):c.62A>G (p.Lys21Arg)	INMT-MINDY4, LOC113748388 +1 more (K21R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126622	NM_032222.3(MINDY4):c.554T>G (p.Leu185Arg)	INMT-MINDY4, MINDY4 (L185R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126621	NM_032222.3(MINDY4):c.545T>C (p.Ile182Thr)	INMT-MINDY4, MINDY4 (I182T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3126620	NM_032222.3(MINDY4):c.476C>T (p.Pro159Leu)	INMT-MINDY4, MINDY4 (P159L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126619	NM_032222.3(MINDY4):c.422A>G (p.His141Arg)	INMT-MINDY4, MINDY4 (H141R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126618	NM_032222.3(MINDY4):c.340A>T (p.Thr114Ser)	INMT-MINDY4, MINDY4 (T114S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126617	NM_032222.3(MINDY4):c.2182G>C (p.Asp728His)	INMT-MINDY4, MINDY4 (D728H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126616	NM_032222.3(MINDY4):c.2161C>G (p.Gln721Glu)	INMT-MINDY4, MINDY4 (Q721E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126615	NM_032222.3(MINDY4):c.2069G>A (p.Arg690His)	INMT-MINDY4, MINDY4 (R690H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126614	NM_032222.3(MINDY4):c.2068C>T (p.Arg690Cys)	INMT-MINDY4, MINDY4 (R690C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126613	NM_032222.3(MINDY4):c.2048G>T (p.Ser683Ile)	INMT-MINDY4, MINDY4 (S683I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126612	NM_032222.3(MINDY4):c.2025G>C (p.Glu675Asp)	INMT-MINDY4, MINDY4 (E675D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126611	NM_032222.3(MINDY4):c.1984C>G (p.Leu662Val)	INMT-MINDY4, MINDY4 (L662V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126610	NM_032222.3(MINDY4):c.1912A>G (p.Ile638Val)	INMT-MINDY4, MINDY4 (I638V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126609	NM_032222.3(MINDY4):c.190G>A (p.Glu64Lys)	INMT-MINDY4, MINDY4 (E64K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126608	NM_032222.3(MINDY4):c.1889G>A (p.Gly630Glu)	INMT-MINDY4, MINDY4 (G630E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126607	NM_032222.3(MINDY4):c.1850A>G (p.Asn617Ser)	INMT-MINDY4, MINDY4 (N617S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126606	NM_032222.3(MINDY4):c.1826T>A (p.Leu609His)	INMT-MINDY4, MINDY4 (L609H)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126605	NM_032222.3(MINDY4):c.1750C>T (p.Arg584Cys)	INMT-MINDY4, MINDY4 (R584C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126604	NM_032222.3(MINDY4):c.1693T>G (p.Tyr565Asp)	INMT-MINDY4, MINDY4 (Y565D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126603	NM_032222.3(MINDY4):c.1610C>A (p.Thr537Lys)	INMT-MINDY4, MINDY4 (T537K)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126602	NM_032222.3(MINDY4):c.1553C>T (p.Ser518Leu)	INMT-MINDY4, MINDY4 (S518L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126601	NM_032222.3(MINDY4):c.1526G>A (p.Arg509Gln)	INMT-MINDY4, MINDY4 (R509Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126600	NM_032222.3(MINDY4):c.1514G>A (p.Arg505Gln)	INMT-MINDY4, MINDY4 (R505Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126599	NM_032222.3(MINDY4):c.1501G>A (p.Asp501Asn)	INMT-MINDY4, MINDY4 (D501N)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126598	NM_032222.3(MINDY4):c.1456C>G (p.Pro486Ala)	INMT-MINDY4, MINDY4 (P486A)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126597	NM_032222.3(MINDY4):c.1433C>T (p.Ala478Val)	INMT-MINDY4, MINDY4 (A478V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126596	NM_032222.3(MINDY4):c.136G>T (p.Asp46Tyr)	INMT-MINDY4, MINDY4 (D46Y)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126595	NM_032222.3(MINDY4):c.1340G>A (p.Gly447Asp)	INMT-MINDY4, MINDY4 (G447D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126594	NM_032222.3(MINDY4):c.1175C>G (p.Ser392Trp)	INMT-MINDY4, MINDY4 (S392W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126593	NM_032222.3(MINDY4):c.1109G>A (p.Gly370Asp)	INMT-MINDY4, MINDY4 (G370D)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 3126592	NM_032222.3(MINDY4):c.106C>T (p.Arg36Cys)	INMT-MINDY4, MINDY4 (R36C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126591	NM_032222.3(MINDY4):c.1045C>T (p.Arg349Trp)	INMT-MINDY4, MINDY4 (R349W)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3126590	NM_032222.3(MINDY4):c.1012A>G (p.Met338Val)	INMT-MINDY4, MINDY4 (M338V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2657375	NM_032222.3(MINDY4):c.1617G>A (p.Thr539=)	INMT-MINDY4, MINDY4	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2657374	NM_032222.3(MINDY4):c.144A>G (p.Arg48=)	INMT-MINDY4, MINDY4	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GLikely benign
Select item 2620963	NM_032222.3(MINDY4):c.1043A>G (p.Lys348Arg)	INMT-MINDY4, MINDY4 (K348R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2616477	NM_032222.3(MINDY4):c.2068C>G (p.Arg690Gly)	INMT-MINDY4, MINDY4 (R690G)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2607288	NM_032222.3(MINDY4):c.1421G>A (p.Gly474Glu)	INMT-MINDY4, MINDY4 (G474E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2604657	NM_032222.3(MINDY4):c.757G>T (p.Val253Phe)	INMT-MINDY4, MINDY4 (V253F)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2596884	NM_032222.3(MINDY4):c.683A>G (p.Tyr228Cys)	INMT-MINDY4, MINDY4 (Y228C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2557106	NM_032222.3(MINDY4):c.1486G>A (p.Val496Ile)	INMT-MINDY4, MINDY4 (V496I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2547304	NM_032222.3(MINDY4):c.190G>C (p.Glu64Gln)	INMT-MINDY4, MINDY4 (E64Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2526288	NM_032222.3(MINDY4):c.1091C>T (p.Pro364Leu)	INMT-MINDY4, MINDY4 (P364L)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2476266	NM_032222.3(MINDY4):c.1516G>A (p.Ala506Thr)	INMT-MINDY4, MINDY4 (A506T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2470113	NM_032222.3(MINDY4):c.292C>A (p.Leu98Ile)	INMT-MINDY4, MINDY4 (L98I)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2467079	NM_032222.3(MINDY4):c.1616C>T (p.Thr539Met)	INMT-MINDY4, MINDY4 (T539M)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2463650	NM_032222.3(MINDY4):c.305A>G (p.Lys102Arg)	INMT-MINDY4, MINDY4 (K102R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2462766	NM_032222.3(MINDY4):c.1930A>G (p.Ile644Val)	INMT-MINDY4, MINDY4 (I644V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2461218	NM_032222.3(MINDY4):c.1859A>G (p.Asn620Ser)	INMT-MINDY4, MINDY4 (N620S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2459292	NM_032222.3(MINDY4):c.100C>T (p.Arg34Cys)	INMT-MINDY4, MINDY4 (R34C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance

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Items: 61