"CeGaT Center for Human Genetics Tuebingen"[submitter] AND "KRT10"[gen - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 808260	NM_000421.5(KRT10):c.1639_1653dup (p.543GGGSS[3])	KRT10	Duplication (inframe_insertion)	not provided +1 more	GBenign/Likely benign
Select item 1335270	NM_000421.5(KRT10):c.1632C>A (p.Gly544=)	KRT10	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 2647747	NM_000421.5(KRT10):c.1560C>T (p.Gly520=)	KRT10	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2647748	NM_000421.5(KRT10):c.1559G>T (p.Gly520Val)	KRT10 (G520V)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2084433	NM_000421.5(KRT10):c.789C>T (p.Thr263=)	KRT10, KRT10-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1013386	NM_000421.5(KRT10):c.759C>T (p.Asn253=)	KRT10, KRT10-AS1 +1 more	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2084352	NM_000421.5(KRT10):c.321C>T (p.Phe107=)	KRT10, KRT10-AS1	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1013387	NM_000421.5(KRT10):c.257G>A (p.Arg86His)	KRT10, KRT10-AS1 (R86H)	Single nucleotide variant (missense variant)	KRT10-related condition +1 more	GBenign/Likely benign
Select item 444403	NM_000421.5(KRT10):c.158G>A (p.Ser53Asn)	KRT10, KRT10-AS1 (S53N)	Single nucleotide variant (missense variant)	not provided	GUncertain significance