Related gene-specific medical variations for Gene (Select 23637) - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3101683	NM_005294.3(GPR21):c.71C>G (p.Thr24Ser)	GPR21, RABGAP1 (T24S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101682	NM_005294.3(GPR21):c.505G>T (p.Gly169Cys)	GPR21, RABGAP1 (G169C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101681	NM_005294.3(GPR21):c.412A>G (p.Asn138Asp)	GPR21, RABGAP1 (N138D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101680	NM_005294.3(GPR21):c.407C>T (p.Thr136Ile)	GPR21, RABGAP1 (T136I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101679	NM_005294.3(GPR21):c.190A>G (p.Thr64Ala)	GPR21, RABGAP1 (T64A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3101678	NM_005294.3(GPR21):c.1025G>T (p.Gly342Val)	GPR21, RABGAP1 (G342V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2611432	NM_005294.3(GPR21):c.737C>G (p.Pro246Arg)	GPR21, RABGAP1 (P246R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2589514	NM_005294.3(GPR21):c.967T>C (p.Cys323Arg)	GPR21, RABGAP1 (C323R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2544547	NM_005294.3(GPR21):c.773C>G (p.Thr258Ser)	GPR21, RABGAP1 (T258S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2537961	NM_005294.3(GPR21):c.410A>G (p.Tyr137Cys)	GPR21, RABGAP1 (Y137C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2397115	NM_005294.3(GPR21):c.647G>A (p.Arg216His)	GPR21, RABGAP1 (R216H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2378932	NM_005294.3(GPR21):c.146T>C (p.Val49Ala)	GPR21, RABGAP1 (V49A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2284555	NM_005294.3(GPR21):c.841A>C (p.Ser281Arg)	GPR21, RABGAP1 (S281R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2273751	NM_005294.3(GPR21):c.638A>T (p.Asn213Ile)	GPR21, RABGAP1 (N213I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2267197	NM_005294.3(GPR21):c.551C>T (p.Ser184Phe)	GPR21, RABGAP1 (S184F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2255241	NM_005294.3(GPR21):c.280C>T (p.Leu94Phe)	GPR21, RABGAP1 (L94F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2247541	NM_005294.3(GPR21):c.368T>C (p.Ile123Thr)	GPR21, RABGAP1 (I123T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2234092	NM_005294.3(GPR21):c.1000G>A (p.Asp334Asn)	GPR21, RABGAP1 (D334N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2224117	NM_005294.3(GPR21):c.679G>A (p.Glu227Lys)	GPR21, RABGAP1 (E227K)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign