ClinVar Miner

List of variants in gene LYST reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 33
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_000081.4(LYST):c.5518T>G (p.Ser1840Ala) rs115330112 0.00485
NM_000081.4(LYST):c.8913T>G (p.Asn2971Lys) rs34702903 0.00276
NM_000081.4(LYST):c.2363+4T>C rs201398337 0.00252
NM_000081.4(LYST):c.3683A>G (p.Asn1228Ser) rs145553827 0.00171
NM_000081.4(LYST):c.6710A>C (p.Gln2237Pro) rs138443479 0.00148
NM_000081.4(LYST):c.8027G>T (p.Ser2676Ile) rs113209379 0.00086
NM_000081.4(LYST):c.9017A>G (p.Lys3006Arg) rs140934482 0.00047
NM_000081.4(LYST):c.3208A>G (p.Ile1070Val) rs150321124 0.00043
NM_000081.4(LYST):c.3898A>G (p.Ile1300Val) rs199855658 0.00021
NM_000081.4(LYST):c.8151T>C (p.Ile2717=) rs201045270 0.00012
NM_000081.4(LYST):c.281C>T (p.Thr94Ile) rs777389303 0.00009
NM_000081.4(LYST):c.9520G>A (p.Val3174Ile) rs199672291 0.00008
NM_000081.4(LYST):c.6149G>A (p.Arg2050Gln) rs376311093 0.00006
NM_000081.4(LYST):c.7862T>C (p.Met2621Thr) rs368500877 0.00006
NM_000081.4(LYST):c.1848C>T (p.Asn616=) rs376259384 0.00001
NM_000081.4(LYST):c.3250G>A (p.Ala1084Thr) rs376496670 0.00001
NM_000081.4(LYST):c.5578A>G (p.Met1860Val) rs368738466 0.00001
NM_000081.4(LYST):c.6736C>T (p.Leu2246Phe) rs758716853 0.00001
NM_000081.4(LYST):c.9243A>C (p.Gln3081His) rs757239793 0.00001
NC_000001.10:g.(235856787_235860382)_(236030207_?)dup
NM_000081.4(LYST):c.1691C>T (p.Ala564Val)
NM_000081.4(LYST):c.18C>G (p.Asn6Lys)
NM_000081.4(LYST):c.2304C>G (p.Cys768Trp)
NM_000081.4(LYST):c.2442T>A (p.Ser814Arg)
NM_000081.4(LYST):c.2570C>G (p.Ser857Cys)
NM_000081.4(LYST):c.3256G>A (p.Glu1086Lys)
NM_000081.4(LYST):c.5461-3dup rs557545474
NM_000081.4(LYST):c.5620T>C (p.Phe1874Leu)
NM_000081.4(LYST):c.6331A>G (p.Thr2111Ala)
NM_000081.4(LYST):c.7467C>T (p.Pro2489=) rs797045685
NM_000081.4(LYST):c.7957A>G (p.Arg2653Gly)
NM_000081.4(LYST):c.9315+6T>C
NM_000081.4(LYST):c.9488A>G (p.Tyr3163Cys)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.