ClinVar Miner

List of variants in gene CASP10 reported as benign for immune system disorder

Included ClinVar conditions (908):
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_032977.4(CASP10):c.177A>G (p.Ser59=) rs3900115 0.49172
NM_032977.4(CASP10):c.1564T>A (p.Leu522Ile) rs13006529 0.42733
NM_032977.3(CASP10):c.-206C>T rs16836789 0.12450
NM_032977.4(CASP10):c.*285G>A rs3851974 0.11086
NM_032977.4(CASP10):c.*277G>A rs3931696 0.11064
NM_032977.4(CASP10):c.923-3C>T rs6753900 0.06908
NM_032977.4(CASP10):c.*1920G>C rs11885191 0.06626
NM_032977.3(CASP10):c.-360T>C rs41429849 0.06590
NM_032977.4(CASP10):c.*2757A>G rs13414860 0.06432
NM_032977.4(CASP10):c.1228G>A (p.Val410Ile) rs13010627 0.04350
NM_032977.4(CASP10):c.*815C>T rs17860409 0.03348
NM_032977.4(CASP10):c.685-20C>T rs17860401 0.03338
NM_032977.4(CASP10):c.1337A>G (p.Tyr446Cys) rs17860405 0.02926
NM_032977.4(CASP10):c.*367G>C rs41365346 0.01382
NM_032977.4(CASP10):c.*3513A>G rs6752492 0.00762
NM_032977.4(CASP10):c.*2689A>G rs41447745 0.00601
NM_032977.4(CASP10):c.*2831C>T rs151162733 0.00535
NM_032977.4(CASP10):c.*2289A>C rs41369551 0.00488
NM_032977.4(CASP10):c.*1471G>A rs192319559 0.00466
NM_032977.4(CASP10):c.*665G>A rs142072849 0.00456
NM_032977.4(CASP10):c.*77T>G rs191438878 0.00455
NM_032977.4(CASP10):c.1068G>T (p.Leu356=) rs111489269 0.00455
NM_032977.4(CASP10):c.*3137G>C rs41522046 0.00417
NM_032977.4(CASP10):c.*2618G>A rs41431151 0.00382
NM_032977.4(CASP10):c.*1043C>T rs553212718 0.00334
NM_032977.4(CASP10):c.*1593T>C rs564618271 0.00307
NM_032977.4(CASP10):c.1296C>T (p.Ala432=) rs41331850 0.00298
NM_032977.4(CASP10):c.1415+18T>A rs111608359 0.00274
NM_032977.4(CASP10):c.*1793C>A rs114760847 0.00258
NM_032977.4(CASP10):c.*1955G>A rs139807893 0.00249
NM_032977.4(CASP10):c.*3071G>A rs41339144 0.00247
NM_032977.4(CASP10):c.534A>C (p.Val178=) rs146233833 0.00226
NM_032977.4(CASP10):c.*1688A>G rs41515650 0.00191
NM_032977.4(CASP10):c.722-16G>T rs41500646 0.00121
NM_032977.4(CASP10):c.1502C>T (p.Pro501Leu) rs148939095 0.00091
NM_032977.4(CASP10):c.*1914C>T rs185318287 0.00070
NM_032977.4(CASP10):c.1415+16T>C rs201336330 0.00058
NM_032977.4(CASP10):c.347+8C>T rs140246829 0.00056
NM_032977.4(CASP10):c.-8+5G>A rs781551128 0.00034
NM_032977.4(CASP10):c.1202_1208del (p.Cys401fs) rs747900630 0.00033
NM_032977.4(CASP10):c.*739T>C rs559831804 0.00024
NM_032977.4(CASP10):c.1347T>C (p.Phe449=) rs147814983 0.00021
NM_032977.4(CASP10):c.930G>T (p.Leu310=) rs149096064 0.00020
NM_032977.4(CASP10):c.*230G>A rs565567149 0.00014
NM_032977.4(CASP10):c.1415+8C>G rs200638628 0.00013
NM_032977.4(CASP10):c.666A>G (p.Thr222=) rs116125703 0.00013
NM_032977.4(CASP10):c.20A>G (p.His7Arg) rs200935960 0.00004
NM_032977.4(CASP10):c.*846A>G rs41529249 0.00003
NM_032977.4(CASP10):c.*3019C>T rs548104022 0.00001
NM_032977.4(CASP10):c.49A>G (p.Lys17Glu) rs552561721 0.00001
NM_032977.4(CASP10):c.923-13T>G rs776612061 0.00001
NM_032977.4(CASP10):c.*1520C>T rs41331447
NM_032977.4(CASP10):c.*1982del rs111572089
NM_032977.4(CASP10):c.1415+18del
NM_032977.4(CASP10):c.1415+18dup rs749295497
NM_032977.4(CASP10):c.174C>T (p.Ala58=) rs114625983
NM_032977.4(CASP10):c.347+9G>T rs7608787
NM_032977.4(CASP10):c.348-16dup rs771877930
NM_032977.4(CASP10):c.923-12G>T rs201904750

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