Related gene-specific medical variations for Gene (Select 142685) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3130141	NM_001290258.2(ASB15):c.89C>T (p.Thr30Ile)	ASB15, ASB15-AS1 (T30I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130134	NM_001290258.2(ASB15):c.512A>G (p.Asp171Gly)	ASB15, ASB15-AS1 (D171G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130133	NM_001290258.2(ASB15):c.427A>G (p.Lys143Glu)	ASB15, ASB15-AS1 (K143E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130132	NM_001290258.2(ASB15):c.370G>A (p.Val124Met)	ASB15, ASB15-AS1 (V124M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130131	NM_001290258.2(ASB15):c.355G>C (p.Val119Leu)	ASB15, ASB15-AS1 (V119L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3130130	NM_001290258.2(ASB15):c.207G>A (p.Met69Ile)	ASB15, ASB15-AS1 (M69I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2612779	NM_001290258.2(ASB15):c.118C>G (p.Leu40Val)	ASB15, ASB15-AS1 (L40V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2595791	NM_001290258.2(ASB15):c.574A>C (p.Ile192Leu)	ASB15, ASB15-AS1 (I192L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558970	NM_001290258.2(ASB15):c.598G>A (p.Gly200Arg)	ASB15, ASB15-AS1 (G200R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2263393	NM_001290258.2(ASB15):c.662G>T (p.Gly221Val)	ASB15, ASB15-AS1 (G221V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260247	NM_001290258.2(ASB15):c.226G>A (p.Gly76Arg)	ASB15, ASB15-AS1 (G76R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2259049	NM_001290258.2(ASB15):c.31C>T (p.His11Tyr)	ASB15, ASB15-AS1 (H11Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance