List of variants in gene KRT16 reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 29

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HGVS	dbSNP	gnomAD frequency
NM_005557.4(KRT16):c.1281-16T>C	rs7406899	0.96977
NM_005557.4(KRT16):c.624T>C (p.His208=)	rs4796681	0.66007
NM_005557.4(KRT16):c.558G>A (p.Ala186=)	rs144914208	0.02243
NM_005557.4(KRT16):c.67G>A (p.Gly23Ser)	rs7226192	0.01897
NM_005557.4(KRT16):c.121C>T (p.Arg41Cys)	rs111383277	0.01598
NM_005557.4(KRT16):c.212G>C (p.Gly71Ala)	rs144088254	0.00921
NM_005557.4(KRT16):c.1252C>T (p.Arg418Cys)	rs56259134	0.00512
NM_005557.4(KRT16):c.199G>A (p.Gly67Ser)	rs62066634	0.00450
NM_005557.4(KRT16):c.644C>G (p.Thr215Ser)	rs147423442	0.00299
NM_005557.4(KRT16):c.771+3A>G	rs113890856	0.00255
NM_005557.4(KRT16):c.916A>G (p.Thr306Ala)	rs112891689	0.00244
NM_005557.4(KRT16):c.927G>A (p.Leu309=)	rs113500657	0.00243
NM_005557.4(KRT16):c.1168C>T (p.Arg390Cys)	rs141569849	0.00219
NM_005557.4(KRT16):c.246C>T (p.Phe82=)	rs377639708	0.00146
NM_005557.4(KRT16):c.539C>T (p.Ala180Val)	rs142750223	0.00131
NM_005557.4(KRT16):c.336T>C (p.Leu112=)	rs145042222	0.00112
NM_005557.4(KRT16):c.699C>T (p.Ala233=)	rs138889840	0.00077
NM_005557.4(KRT16):c.674G>A (p.Arg225Gln)	rs142812826	0.00070
NM_005557.4(KRT16):c.637C>T (p.Arg213Trp)	rs148173278	0.00060
NM_005557.4(KRT16):c.933+10G>A	rs371718644	0.00056
NM_005557.4(KRT16):c.933+15C>T	rs373253568	0.00045
NM_005557.4(KRT16):c.1343C>T (p.Ser448Leu)	rs148936519	0.00037
NM_005557.4(KRT16):c.135C>T (p.Thr45=)	rs200661306	0.00037
NM_005557.4(KRT16):c.596C>T (p.Ala199Val)	rs144984779	0.00034
NM_005557.4(KRT16):c.1225C>T (p.Arg409Trp)
NM_005557.4(KRT16):c.207C>T (p.Gly69=)	rs112223718
NM_005557.4(KRT16):c.444G>A (p.Lys148=)	rs149934946
NM_005557.4(KRT16):c.588G>A (p.Arg196=)	rs570955567
NM_005557.4(KRT16):c.989G>T (p.Arg330Leu)	rs140407898

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