Related gene-specific medical variations for Gene (Select 11108) - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623995	NM_012406.4(PRDM4):c.779A>G (p.Asn260Ser)	PRDM4, PRDM4-AS1 (N260S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615429	NM_012406.4(PRDM4):c.1145G>A (p.Arg382His)	PRDM4, PRDM4-AS1 (R382H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2610900	NM_012406.4(PRDM4):c.1919A>C (p.His640Pro)	PRDM4, PRDM4-AS1 (H640P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2602091	NM_012406.4(PRDM4):c.727A>C (p.Asn243His)	PRDM4, PRDM4-AS1 (N243H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2591372	NM_012406.4(PRDM4):c.1206A>G (p.Ile402Met)	PRDM4, PRDM4-AS1 (I402M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2589752	NM_012406.4(PRDM4):c.1837A>G (p.Met613Val)	PRDM4, PRDM4-AS1 (M613V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2559379	NM_012406.4(PRDM4):c.1950G>C (p.Leu650Phe)	PRDM4, PRDM4-AS1 (L650F)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2537191	NM_012406.4(PRDM4):c.267C>G (p.Asn89Lys)	PRDM4, PRDM4-AS1 (N89K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2522749	NM_012406.4(PRDM4):c.154G>C (p.Val52Leu)	PRDM4, PRDM4-AS1 (V52L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2480456	NM_012406.4(PRDM4):c.1589G>A (p.Arg530Gln)	PRDM4, PRDM4-AS1 (R530Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2469786	NM_012406.4(PRDM4):c.886A>G (p.Thr296Ala)	PRDM4, PRDM4-AS1 (T296A)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2460323	NM_012406.4(PRDM4):c.1014G>C (p.Met338Ile)	PRDM4, PRDM4-AS1 (M338I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2361526	NM_012406.4(PRDM4):c.847A>G (p.Ser283Gly)	PRDM4-AS1, PRDM4 (S283G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2352467	NM_012406.4(PRDM4):c.833A>G (p.Asn278Ser)	PRDM4, PRDM4-AS1 (N278S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2335874	NM_012406.4(PRDM4):c.840G>A (p.Met280Ile)	PRDM4-AS1, PRDM4 (M280I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2320967	NM_012406.4(PRDM4):c.853C>G (p.Leu285Val)	PRDM4-AS1, PRDM4 (L285V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2260480	NM_012406.4(PRDM4):c.520G>T (p.Gly174Cys)	PRDM4-AS1, PRDM4 (G174C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2254990	NM_012406.4(PRDM4):c.1487G>A (p.Arg496Gln)	PRDM4, PRDM4-AS1 (R496Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2252007	NM_012406.4(PRDM4):c.1396A>T (p.Ile466Leu)	PRDM4-AS1, PRDM4 (I466L)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2240172	NM_012406.4(PRDM4):c.1913A>G (p.Lys638Arg)	PRDM4-AS1, PRDM4 (K638R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2237549	NM_012406.4(PRDM4):c.1157C>G (p.Ser386Trp)	PRDM4, PRDM4-AS1 (S386W)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2237290	NM_012406.4(PRDM4):c.1753A>G (p.Ser585Gly)	PRDM4-AS1, PRDM4 (S585G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2231919	NM_012406.4(PRDM4):c.502C>T (p.Arg168Cys)	PRDM4, PRDM4-AS1 (R168C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220457	NM_012406.4(PRDM4):c.2053C>T (p.Arg685Trp)	PRDM4-AS1, PRDM4 (R685W)	Single nucleotide variant (non-coding transcript variant +1 more)	Inborn genetic diseases	GUncertain significance
Select item 2218312	NM_012406.4(PRDM4):c.1307G>A (p.Arg436Gln)	PRDM4, PRDM4-AS1 (R436Q)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance

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Links from Gene

Items: 25