Related gene-specific medical variations for Gene (Select 63917) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3280534	NM_022087.4(GALNT11):c.838G>A (p.Asp280Asn)	GALNT11, LOC126860227 (D199N +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3280531	NM_022087.4(GALNT11):c.917C>T (p.Pro306Leu)	GALNT11, LOC126860227 (P207L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3098059	NM_022087.4(GALNT11):c.922T>C (p.Ser308Pro)	GALNT11, LOC126860227 (S308P +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3098058	NM_022087.4(GALNT11):c.774G>T (p.Leu258Phe)	GALNT11, LOC126860227 (L216F +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2339160	NM_022087.4(GALNT11):c.926A>T (p.Glu309Val)	GALNT11, LOC126860227 (E210V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291113	NM_022087.4(GALNT11):c.946G>A (p.Ala316Thr)	GALNT11, LOC126860227 (A235T +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235307	NM_022087.4(GALNT11):c.788G>A (p.Arg263His)	GALNT11, LOC126860227 (R164H +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

ClinVar