Related gene-specific medical variations for Gene (Select 55843) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3310916	NM_018460.4(ARHGAP15):c.1373T>C (p.Ile458Thr)	ARHGAP15, ARHGAP15-AS1 (I458T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3128517	NM_018460.4(ARHGAP15):c.1208G>A (p.Arg403His)	ARHGAP15, ARHGAP15-AS1 (R403H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597142	NM_018460.4(ARHGAP15):c.1372A>G (p.Ile458Val)	ARHGAP15, ARHGAP15-AS1 (I458V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528081	NM_018460.4(ARHGAP15):c.1225C>T (p.Leu409Phe)	ARHGAP15, ARHGAP15-AS1 (L409F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386885	NM_018460.4(ARHGAP15):c.1159A>G (p.Arg387Gly)	ARHGAP15, ARHGAP15-AS1 (R387G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2371802	NM_018460.4(ARHGAP15):c.1319G>A (p.Arg440Gln)	ARHGAP15, ARHGAP15-AS1 (R440Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351380	NM_018460.4(ARHGAP15):c.1199C>T (p.Pro400Leu)	ARHGAP15, ARHGAP15-AS1 (P400L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2258437	NM_018460.4(ARHGAP15):c.1364A>G (p.Gln455Arg)	ARHGAP15, ARHGAP15-AS1 (Q455R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248739	NM_018460.4(ARHGAP15):c.1354A>G (p.Met452Val)	ARHGAP15, ARHGAP15-AS1 (M452V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216091	NM_018460.4(ARHGAP15):c.1280C>T (p.Thr427Met)	ARHGAP15, ARHGAP15-AS1 (T427M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808969	GRCh37/hg19 2q22.3(chr2:144192888-144248006)x1	ARHGAP15	Copy number loss	not provided	GUncertain significance