ClinVar Miner

List of variants reported as benign for integumentary system benign neoplasm by Illumina Laboratory Services, Illumina

Included ClinVar conditions (37):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 75
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HGVS dbSNP gnomAD frequency
NM_002272.4(KRT4):c.1346+15A>G rs931479 0.83879
NM_153490.3(KRT13):c.735+10A>G rs7211835 0.83623
NM_002272.4(KRT4):c.678-14G>A rs2307027 0.83484
NM_002272.4(KRT4):c.*269A>G rs2035879 0.82793
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_002272.4(KRT4):c.215C>T (p.Ala72Val) rs2638525 0.51489
NM_002272.4(KRT4):c.467A>G (p.Gln156Arg) rs7959052 0.28838
NM_153490.3(KRT13):c.437C>G (p.Ala146Gly) rs760134 0.07279
NM_153490.3(KRT13):c.*170C>T rs3169911 0.05973
NM_002272.4(KRT4):c.1381+15C>T rs7952923 0.03297
NM_002272.4(KRT4):c.261T>A (p.Gly87=) rs74445207 0.02489
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_002272.4(KRT4):c.*133C>T rs78282727 0.01188
NM_002272.4(KRT4):c.122G>A (p.Arg41Gln) rs36143766 0.01050
NM_002272.4(KRT4):c.678-3C>T rs73306189 0.01050
NM_002272.4(KRT4):c.404C>T (p.Thr135Met) rs17119475 0.01042
NM_002272.4(KRT4):c.267T>C (p.Phe89=) rs372168510 0.01016
NM_002272.4(KRT4):c.288G>A (p.Lys96=) rs372013854 0.00989
NM_153490.3(KRT13):c.177T>C (p.Ser59=) rs142246675 0.00900
NM_153490.3(KRT13):c.735+6C>T rs181122697 0.00469
NM_002272.4(KRT4):c.456C>T (p.Ile152=) rs140582332 0.00421
NM_002272.4(KRT4):c.870G>A (p.Thr290=) rs189596654 0.00376
NM_002272.4(KRT4):c.*81T>A rs572216995 0.00279
NM_002272.4(KRT4):c.623G>A (p.Arg208His) rs201795280 0.00223
NM_002272.4(KRT4):c.*68C>T rs149040467 0.00159
NM_153490.3(KRT13):c.1276G>A (p.Val426Ile) rs144967807 0.00157
NM_002272.4(KRT4):c.1258C>T (p.Arg420Cys) rs192699667 0.00134
NM_002272.4(KRT4):c.1080G>A (p.Arg360=) rs113928381 0.00131
NM_002272.4(KRT4):c.306C>T (p.Pro102=) rs373594963 0.00121
NM_153490.3(KRT13):c.*274T>C rs141918873 0.00117
NM_002272.4(KRT4):c.1203C>T (p.Arg401=) rs199607128 0.00103
NM_002272.4(KRT4):c.361C>A (p.Pro121Thr) rs200831095 0.00094
NM_153490.3(KRT13):c.509C>G (p.Thr170Ser) rs148102980 0.00087
NM_002272.4(KRT4):c.1318C>T (p.Arg440Cys) rs200484321 0.00081
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_002272.4(KRT4):c.1495G>C (p.Gly499Arg) rs190897990 0.00056
NM_002272.4(KRT4):c.224G>A (p.Gly75Glu) rs200665579 0.00041
NM_153490.3(KRT13):c.1009T>C (p.Ser337Pro) rs139318123 0.00041
NM_002272.4(KRT4):c.548A>G (p.Asn183Ser) rs199768158 0.00039
NM_002272.4(KRT4):c.766G>A (p.Val256Met) rs201754946 0.00035
NM_002272.4(KRT4):c.*30T>A rs372075566 0.00033
NM_153490.3(KRT13):c.1366C>T (p.Arg456Cys) rs146666963 0.00029
NM_002272.4(KRT4):c.1493T>C (p.Phe498Ser) rs377399080 0.00024
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_002272.4(KRT4):c.873C>T (p.Ser291=) rs754647771 0.00011
NM_153490.3(KRT13):c.*268C>T rs188347004 0.00011
NM_002272.4(KRT4):c.1419C>T (p.Ser473=) rs534019513 0.00010
NM_002272.4(KRT4):c.475G>A (p.Glu159Lys) rs188245182 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_002272.4(KRT4):c.31G>A (p.Gly11Arg) rs371421345 0.00008
NM_002272.4(KRT4):c.-51G>A rs531951809 0.00006
NM_153490.3(KRT13):c.1133G>A (p.Arg378His) rs200309164 0.00005
NM_002272.4(KRT4):c.1512C>A (p.Gly504=) rs573971498 0.00004
NM_153490.3(KRT13):c.869G>A (p.Arg290Gln) rs535020030 0.00004
NM_002272.4(KRT4):c.835-4G>T rs767441876 0.00003
NM_002272.4(KRT4):c.983C>T (p.Ala328Val) rs749943854 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_002272.4(KRT4):c.*267G>A rs546884677 0.00002
NM_153490.3(KRT13):c.1352G>A (p.Arg451His) rs550693344 0.00002
NM_002272.4(KRT4):c.558C>G (p.Pro186=) rs766644080 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_002272.4(KRT4):c.1020G>C (p.Ser340=) rs7956809
NM_002272.4(KRT4):c.1259G>A (p.Arg420His) rs377329227
NM_153490.3(KRT13):c.1217G>T (p.Arg406Leu) rs145983286
NM_153490.3(KRT13):c.1286G>A (p.Arg429His) rs150321809

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