Related gene-specific medical variations for Gene (Select 81502) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106188	NM_178581.3(HM13):c.1133A>C (p.Gln378Pro)	HM13, HM13-AS1 (Q378P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2603355	NM_178581.3(HM13):c.1160G>A (p.Arg387His)	HM13, HM13-AS1 (R387H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2377530	NM_178581.3(HM13):c.1163C>T (p.Pro388Leu)	HM13, HM13-AS1 (P388L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2372421	NM_178581.3(HM13):c.1177G>A (p.Ala393Thr)	HM13, HM13-AS1 (A393T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2370086	NM_178581.3(HM13):c.1120G>A (p.Asp374Asn)	HM13, HM13-AS1 (D374N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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