GAB4[gene] and "single gene"[properties] - ClinVar

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Items: 43

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2623195	NM_001037814.1(GAB4):c.1649A>T (p.Gln550Leu)	GAB4 (Q550L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276356	NM_001037814.1(GAB4):c.1609A>G (p.Lys537Glu)	GAB4 (K384E +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2216177	NM_001037814.1(GAB4):c.1537A>C (p.Thr513Pro)	GAB4 (T360P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2213998	NM_001037814.1(GAB4):c.1529C>G (p.Pro510Arg)	GAB4 (P357R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2392920	NM_001037814.1(GAB4):c.1481C>T (p.Pro494Leu)	GAB4 (P494L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097772	NM_001037814.1(GAB4):c.1437C>G (p.Asn479Lys)	GAB4 (N326K +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262790	NM_001037814.1(GAB4):c.1165T>G (p.Cys389Gly)	GAB4 (C236G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2226531	NM_001037814.1(GAB4):c.1152C>G (p.Ile384Met)	GAB4 (I231M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2369883	NM_001037814.1(GAB4):c.1141G>C (p.Gly381Arg)	GAB4 (G228R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2258542	NM_001037814.1(GAB4):c.1111G>T (p.Ala371Ser)	GAB4 (A218S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2394834	NM_001037814.1(GAB4):c.1109C>T (p.Pro370Leu)	GAB4 (P370L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3097771	NM_001037814.1(GAB4):c.1094G>C (p.Gly365Ala)	GAB4 (G212A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361755	NM_001037814.1(GAB4):c.938C>T (p.Ala313Val)	GAB4 (A160V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2218199	NM_001037814.1(GAB4):c.931A>T (p.Asn311Tyr)	GAB4 (N311Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097784	NM_001037814.1(GAB4):c.929A>T (p.Asp310Val)	GAB4 (D310V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2375596	NM_001037814.1(GAB4):c.926C>T (p.Ala309Val)	GAB4 (A309V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2398629	NM_001037814.1(GAB4):c.910C>T (p.Leu304Phe)	GAB4 (L304F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2212204	NM_001037814.1(GAB4):c.907A>G (p.Ser303Gly)	GAB4 (S303G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2301178	NM_001037814.1(GAB4):c.893G>A (p.Gly298Asp)	GAB4 (G298D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097782	NM_001037814.1(GAB4):c.872C>T (p.Pro291Leu)	GAB4 (P291L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097781	NM_001037814.1(GAB4):c.871C>T (p.Pro291Ser)	GAB4 (P291S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460983	NM_001037814.1(GAB4):c.866G>T (p.Arg289Ile)	GAB4 (R289I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097780	NM_001037814.1(GAB4):c.835C>T (p.His279Tyr)	GAB4 (H279Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2361342	NM_001037814.1(GAB4):c.824A>G (p.Lys275Arg)	GAB4 (K275R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097779	NM_001037814.1(GAB4):c.808T>G (p.Phe270Val)	GAB4 (F270V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097778	NM_001037814.1(GAB4):c.799A>C (p.Ile267Leu)	GAB4 (I267L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097777	NM_001037814.1(GAB4):c.775A>G (p.Ser259Gly)	GAB4 (S259G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2366502	NM_001037814.1(GAB4):c.724A>T (p.Ile242Phe)	GAB4 (I242F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2588876	NM_001037814.1(GAB4):c.661G>A (p.Ala221Thr)	GAB4 (A221T)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2298847	NM_001037814.1(GAB4):c.643C>T (p.Leu215Phe)	GAB4 (L215F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3097776	NM_001037814.1(GAB4):c.635C>T (p.Pro212Leu)	GAB4 (P212L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2319176	NM_001037814.1(GAB4):c.632C>T (p.Pro211Leu)	GAB4 (P211L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2358837	NM_001037814.1(GAB4):c.629C>T (p.Ala210Val)	GAB4 (A210V)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3097775	NM_001037814.1(GAB4):c.608C>T (p.Pro203Leu)	GAB4 (P203L)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2620542	NM_001037814.1(GAB4):c.449T>A (p.Ile150Asn)	GAB4 (I150N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491031	NM_001037814.1(GAB4):c.422A>G (p.Asn141Ser)	GAB4 (N141S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239527	NM_001037814.1(GAB4):c.422A>C (p.Asn141Thr)	GAB4 (N141T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2552519	NM_001037814.1(GAB4):c.371A>G (p.Lys124Arg)	GAB4 (K124R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2548183	NM_001037814.1(GAB4):c.218G>A (p.Ser73Asn)	GAB4 (S73N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2490067	NM_001037814.1(GAB4):c.172T>C (p.Phe58Leu)	GAB4 (F58L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097773	NM_001037814.1(GAB4):c.148C>A (p.Pro50Thr)	GAB4 (P50T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559362	NM_001037814.1(GAB4):c.131G>A (p.Gly44Asp)	GAB4 (G44D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097774	NM_001037814.1(GAB4):c.48C>G (p.Asp16Glu)	GAB4 (D16E)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 43