Related gene-specific medical variations for Gene (Select 3885) - ClinVar - NCBI

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Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3289434	NM_001386014.1(KRT34):c.325A>C (p.Thr109Pro)	KRT34, LOC126862563 (T109P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289431	NM_001386014.1(KRT34):c.392T>C (p.Ile131Thr)	KRT34, LOC126862563 (I131T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3289430	NM_001386014.1(KRT34):c.44G>C (p.Ser15Thr)	KRT34, LOC126862563 (S15T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
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