List of variants in gene CASP10 reported as benign by Illumina Laboratory Services, Illumina

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: 47

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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.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.*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.*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.*1914C>T	rs185318287	0.00070
NM_032977.4(CASP10):c.347+8C>T	rs140246829	0.00056
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.174C>T (p.Ala58=)	rs114625983
NM_032977.4(CASP10):c.347+9G>T	rs7608787
NM_032977.4(CASP10):c.923-12G>T	rs201904750

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