List of variants in gene KRT16 reported as likely 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: 35

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HGVS	dbSNP	gnomAD frequency
NM_005557.4(KRT16):c.1062A>T (p.Lys354Asn)	rs59328451	0.00107
NM_005557.4(KRT16):c.337del (p.Leu113fs)	rs540377400	0.00084
NM_005557.4(KRT16):c.887T>C (p.Met296Thr)	rs145649029	0.00056
NM_005557.4(KRT16):c.925C>T (p.Leu309=)	rs142668383	0.00056
NM_005557.4(KRT16):c.306T>G (p.Phe102Leu)	rs151282702	0.00049
NM_005557.4(KRT16):c.299C>G (p.Ala100Gly)	rs140537366	0.00017
NM_005557.4(KRT16):c.746C>T (p.Ala249Val)	rs373296526	0.00017
NM_005557.4(KRT16):c.837C>T (p.Gly279=)	rs368580381	0.00015
NM_005557.4(KRT16):c.1255C>T (p.Arg419Cys)	rs138335461	0.00012
NM_005557.4(KRT16):c.1097G>A (p.Gly366Asp)	rs150916635	0.00009
NM_005557.4(KRT16):c.933+18del	rs758953756	0.00007
NM_005557.4(KRT16):c.879C>T (p.Tyr293=)	rs767040023	0.00004
NM_005557.4(KRT16):c.909C>T (p.Asp303=)	rs748022914	0.00004
NM_005557.4(KRT16):c.933+13C>G	rs753274079	0.00004
NM_005557.4(KRT16):c.138C>T (p.Tyr46=)	rs377057928	0.00003
NM_005557.4(KRT16):c.144C>T (p.Gly48=)	rs879050220	0.00003
NM_005557.4(KRT16):c.798C>T (p.Thr266=)	rs758059131	0.00003
NM_005557.4(KRT16):c.198C>T (p.Gly66=)	rs142717659	0.00002
NM_005557.4(KRT16):c.429C>T (p.Ala143=)	rs754813514	0.00002
NM_005557.4(KRT16):c.934-8T>C	rs930200593	0.00002
NM_005557.4(KRT16):c.1060-5T>G	rs2508753439	0.00001
NM_005557.4(KRT16):c.769G>A (p.Glu257Lys)	rs778174614	0.00001
NM_005557.4(KRT16):c.1009C>T (p.Arg337Trp)
NM_005557.4(KRT16):c.108C>G (p.Ala36=)	rs774260784
NM_005557.4(KRT16):c.1248C>T (p.Thr416=)
NM_005557.4(KRT16):c.1328-18_1328-16del	rs1477343214
NM_005557.4(KRT16):c.1357C>T (p.Arg453Cys)	rs150387381
NM_005557.4(KRT16):c.1401C>T (p.Phe467=)
NM_005557.4(KRT16):c.207C>A (p.Gly69=)	rs112223718
NM_005557.4(KRT16):c.282C>T (p.Phe94=)	rs570977410
NM_005557.4(KRT16):c.54C>A (p.Cys18Ter)	rs184161015
NM_005557.4(KRT16):c.54C>T (p.Cys18=)	rs184161015
NM_005557.4(KRT16):c.60C>T (p.Ile20=)	rs748848000
NM_005557.4(KRT16):c.747C>T (p.Ala249=)
NM_005557.4(KRT16):c.969C>T (p.Ser323=)	rs759945966

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