Related gene-specific medical variations for Gene (Select 100874365) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3106664	NM_017409.4(HOXC10):c.259C>A (p.Arg87Ser)	HOXC-AS3, HOXC10 (R87S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2516107	NM_017409.4(HOXC10):c.142G>A (p.Gly48Arg)	HOXC-AS3, HOXC10 (G48R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2380449	NM_017409.4(HOXC10):c.193G>A (p.Ala65Thr)	HOXC-AS3, HOXC10 (A65T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365160	NM_017409.4(HOXC10):c.247A>C (p.Lys83Gln)	HOXC-AS3, HOXC10 (K83Q)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2334979	NM_017409.4(HOXC10):c.253G>T (p.Ala85Ser)	HOXC-AS3, HOXC10 (A85S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2241537	NM_017409.4(HOXC10):c.167G>T (p.Arg56Met)	HOXC-AS3, HOXC10 (R56M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 718767	NM_017409.4(HOXC10):c.252C>T (p.Ala84=)	HOXC-AS3, HOXC10	Single nucleotide variant (non-coding transcript variant +1 more)	not provided	GBenign

ClinVar