"PreventionGenetics, part of Exact Sciences"[submitter] AND "KRT6C"[ge - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3053196	NM_173086.5(KRT6C):c.1694A>G (p.Ter565=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder	GLikely benign
Select item 2721628	NM_173086.5(KRT6C):c.1630G>A (p.Gly544Ser)	KRT6C (G544S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign/Likely benign
Select item 1300090	NM_173086.5(KRT6C):c.1503C>T (p.Ser501=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +2 more	GBenign
Select item 1300091	NM_173086.5(KRT6C):c.1460-10C>A	KRT6C	Single nucleotide variant (intron variant)	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse +2 more	GBenign
Select item 1300092	NM_173086.5(KRT6C):c.1441G>A (p.Val481Ile)	KRT6C (V481I)	Single nucleotide variant (missense variant)	KRT6C-related disorder +2 more	GBenign
Select item 2722165	NM_173086.5(KRT6C):c.1434C>T (p.Gly478=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +1 more	GBenign/Likely benign
Select item 1300093	NM_173086.5(KRT6C):c.1314G>A (p.Lys438=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +2 more	GBenign
Select item 768547	NM_173086.5(KRT6C):c.1257A>C (p.Ala419=)	KRT6C	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 1632336	NM_173086.5(KRT6C):c.1023C>T (p.Tyr341=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +1 more	GBenign
Select item 3040614	NM_173086.5(KRT6C):c.960A>G (p.Leu320=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder	GLikely benign
Select item 717355	NM_173086.5(KRT6C):c.879T>C (p.Asp293=)	KRT6C	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1300096	NM_173086.5(KRT6C):c.687C>G (p.Val229=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +1 more	GBenign
Select item 3056771	NM_173086.5(KRT6C):c.680G>A (p.Ser227Asn)	KRT6C (S227N)	Single nucleotide variant (missense variant)	KRT6C-related disorder	GBenign
Select item 3039391	NM_173086.5(KRT6C):c.541-6T>C	KRT6C	Single nucleotide variant (intron variant)	KRT6C-related disorder	GLikely benign
Select item 3059266	NM_173086.5(KRT6C):c.332G>A (p.Gly111Asp)	KRT6C (G111D)	Single nucleotide variant (missense variant)	KRT6C-related disorder	GBenign
Select item 3045913	NM_173086.5(KRT6C):c.318C>A (p.Ala106=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder	GLikely benign
Select item 3060577	NM_173086.5(KRT6C):c.262G>A (p.Gly88Arg)	KRT6C (G88R)	Single nucleotide variant (missense variant)	KRT6C-related disorder	GBenign
Select item 1300100	NM_173086.5(KRT6C):c.198C>A (p.Gly66=)	KRT6C	Single nucleotide variant (synonymous variant)	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse +1 more	GBenign
Select item 1300101	NM_173086.5(KRT6C):c.183G>A (p.Leu61=)	KRT6C	Single nucleotide variant (synonymous variant)	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse +1 more	GBenign
Select item 1300102	NM_173086.5(KRT6C):c.181C>T (p.Leu61=)	KRT6C	Single nucleotide variant (synonymous variant)	Palmoplantar keratoderma, nonepidermolytic, focal or diffuse +1 more	GBenign
Select item 1300103	NM_173086.5(KRT6C):c.180T>C (p.Ser60=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder +1 more	GBenign
Select item 3059899	NM_173086.5(KRT6C):c.147T>C (p.Gly49=)	KRT6C	Single nucleotide variant (synonymous variant)	KRT6C-related disorder	GBenign
Select item 3039989	NM_173086.5(KRT6C):c.118C>T (p.Arg40Cys)	KRT6C (R40C)	Single nucleotide variant (missense variant)	KRT6C-related disorder	GLikely benign

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Items: 23