Related gene-specific medical variations for Gene (Select 126862563) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3116475	NM_001386014.1(KRT34):c.371A>G (p.Asn124Ser)	KRT34, LOC126862563 (N124S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116473	NM_001386014.1(KRT34):c.53C>T (p.Ser18Phe)	KRT34, LOC126862563 (S18F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3116472	NM_001386014.1(KRT34):c.26G>A (p.Ser9Asn)	KRT34, LOC126862563 (S9N)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2495850	NM_001386014.1(KRT34):c.-18A>G	KRT34, LOC126862563	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2363536	NM_001386014.1(KRT34):c.367G>C (p.Glu123Gln)	KRT34, LOC126862563 (E123Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297094	NM_001386014.1(KRT34):c.157A>G (p.Asn53Asp)	KRT34, LOC126862563 (N53D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254174	NM_001386014.1(KRT34):c.-59A>C	KRT34, LOC126862563	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2214354	NM_001386014.1(KRT34):c.271C>T (p.Arg91Trp)	KRT34, LOC126862563 (R91W)	Single nucleotide variant (missense variant)	not specified	GLikely benign

ClinVar