List of variants in gene KRT13 reported as benign for benign neoplasm of skin

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_153490.3(KRT13):c.892A>G (p.Thr298Ala)	rs4796697	0.91638
NM_153490.3(KRT13):c.114C>T (p.Ser38=)	rs8182306	0.87031
NM_153490.3(KRT13):c.735+10A>G	rs7211835	0.83623
NM_153490.3(KRT13):c.897+6C>T	rs4796698	0.81266
NM_153490.3(KRT13):c.560C>T (p.Ala187Val)	rs9891361	0.71565
NM_153490.3(KRT13):c.*171G>T	rs903	0.68196
NM_153490.3(KRT13):c.437C>G (p.Ala146Gly)	rs760134	0.07279
NM_153490.3(KRT13):c.*170C>T	rs3169911	0.05973
NM_153490.3(KRT13):c.204C>A (p.Gly68=)	rs113547405	0.02087
NM_153490.3(KRT13):c.736-7C>G	rs34367942	0.01881
NM_153490.3(KRT13):c.384C>T (p.Ala128=)	rs149623369	0.01541
NM_153490.3(KRT13):c.177T>C (p.Ser59=)	rs142246675	0.00900
NM_153490.3(KRT13):c.735+6C>T	rs181122697	0.00469
NM_153490.3(KRT13):c.1276G>A (p.Val426Ile)	rs144967807	0.00157
NM_153490.3(KRT13):c.*274T>C	rs141918873	0.00117
NM_153490.3(KRT13):c.509C>G (p.Thr170Ser)	rs148102980	0.00096
NM_153490.3(KRT13):c.409C>T (p.Arg137Cys)	rs142183272	0.00078
NM_153490.3(KRT13):c.766G>A (p.Gly256Ser)	rs140780704	0.00072
NM_153490.3(KRT13):c.767G>A (p.Gly256Asp)	rs150947773	0.00060
NM_153490.3(KRT13):c.1009T>C (p.Ser337Pro)	rs139318123	0.00041
NM_153490.3(KRT13):c.1366C>T (p.Arg456Cys)	rs146666963	0.00029
NM_153490.3(KRT13):c.765C>T (p.Val255=)	rs147564962	0.00023
NM_153490.3(KRT13):c.947C>T (p.Thr316Ile)	rs753928241	0.00022
NM_153490.3(KRT13):c.*268C>T	rs188347004	0.00011
NM_153490.3(KRT13):c.815G>A (p.Arg272His)	rs142526332	0.00010
NM_153490.3(KRT13):c.637C>T (p.Arg213Trp)	rs78223890	0.00009
NM_153490.3(KRT13):c.1133G>A (p.Arg378His)	rs200309164	0.00005
NM_153490.3(KRT13):c.869G>A (p.Arg290Gln)	rs535020030	0.00004
NM_153490.3(KRT13):c.1028C>T (p.Ala343Val)	rs199762312	0.00003
NM_153490.3(KRT13):c.1227C>T (p.Leu409=)	rs149077503	0.00003
NM_153490.3(KRT13):c.1352G>A (p.Arg451His)	rs550693344	0.00002
NM_153490.3(KRT13):c.420C>T (p.His140=)	rs530596803	0.00001
NM_153490.3(KRT13):c.449G>A (p.Arg150Gln)	rs548070268	0.00001
NM_153490.3(KRT13):c.1217G>T (p.Arg406Leu)	rs145983286
NM_153490.3(KRT13):c.1286G>A (p.Arg429His)	rs150321809

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