ClinVar Miner

List of variants reported as benign for White sponge nevus 2 by Illumina Laboratory Services, Illumina

Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 33
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HGVS dbSNP gnomAD frequency
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.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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