ClinVar Miner

List of variants in gene KRT13 studied for White sponge nevus 2

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 59
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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 0.00087
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.-45C>A rs367712050 0.00029
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.*228C>G rs574184263 0.00022
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.1238A>T (p.Asp413Val) rs200269035 0.00010
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.759G>C (p.Gln253His) rs766894151 0.00004
NM_153490.3(KRT13):c.869G>A (p.Arg290Gln) rs535020030 0.00004
NM_153490.3(KRT13):c.*175G>A rs1459808765 0.00003
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.1350C>T (p.Arg450=) rs140142101 0.00003
NM_153490.3(KRT13):c.291C>T (p.Gly97=) rs747752896 0.00003
NM_153490.3(KRT13):c.991C>T (p.Leu331=) rs771435962 0.00003
NM_153490.3(KRT13):c.1295C>G (p.Ser432Cys) rs1394162514 0.00002
NM_153490.3(KRT13):c.1352G>A (p.Arg451His) rs550693344 0.00002
NM_153490.3(KRT13):c.*74A>C rs886052907 0.00001
NM_153490.3(KRT13):c.1220G>A (p.Ser407Asn) rs1265435884 0.00001
NM_153490.3(KRT13):c.337G>A (p.Asp113Asn) rs886052908 0.00001
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.496-9A>G rs780820686 0.00001
NM_153490.3(KRT13):c.823G>A (p.Ala275Thr) rs767618537 0.00001
NM_153490.3(KRT13):c.844G>A (p.Glu282Lys) rs202057977 0.00001
NM_153490.3(KRT13):c.9C>T (p.Leu3=) rs185787290 0.00001
NM_153490.3(KRT13):c.*162T>C rs1904829902
NM_153490.3(KRT13):c.*19C>T rs760565338
NM_153490.3(KRT13):c.*85C>T rs886052906
NM_153490.3(KRT13):c.1217G>T (p.Arg406Leu) rs145983286
NM_153490.3(KRT13):c.1286G>A (p.Arg429His) rs150321809
NM_153490.3(KRT13):c.332T>C (p.Leu111Pro) rs59897026
NM_153490.3(KRT13):c.356T>C (p.Leu119Pro) rs60440396
NM_153490.3(KRT13):c.523C>G (p.Arg175Gly) rs764088068
NM_153490.3(KRT13):c.610G>A (p.Val204Met) rs138102206
NM_153490.3(KRT13):c.853G>A (p.Ala285Thr) rs1904920258

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