ClinVar Miner

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

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_000081.3(LYST):c.10235G>A (p.Arg3412His)
NM_000081.3(LYST):c.10286T>G (p.Ile3429Ser) rs760815034
NM_000081.3(LYST):c.11354G>A (p.Arg3785His) rs370173269
NM_000081.3(LYST):c.11362C>T (p.Gln3788Ter) rs1558092244
NM_000081.3(LYST):c.3083C>G (p.Ser1028Cys) rs150636017
NM_000081.3(LYST):c.3311G>A (p.Arg1104Gln) rs148299757
NM_000081.3(LYST):c.3461C>G (p.Thr1154Arg) rs756226516
NM_000081.3(LYST):c.3683A>G (p.Asn1228Ser)
NM_000081.3(LYST):c.3710A>T (p.Asp1237Val) rs1215274878
NM_000081.3(LYST):c.4705A>C (p.Asn1569His)
NM_000081.3(LYST):c.5620T>A (p.Phe1874Ile) rs757494655
NM_000081.3(LYST):c.6388G>A (p.Asp2130Asn) rs148371004
NM_000081.3(LYST):c.6737T>G (p.Leu2246Arg) rs200231136
NM_000081.3(LYST):c.7070C>G (p.Ala2357Gly)
NM_000081.3(LYST):c.7184G>T (p.Cys2395Phe) rs760878646
NM_000081.3(LYST):c.7780+2C>T rs760108842
NM_000081.3(LYST):c.7862T>C (p.Met2621Thr)
NM_000081.3(LYST):c.8806G>A (p.Val2936Ile) rs2753327
NM_000081.3(LYST):c.9045-13T>C
NM_000081.3(LYST):c.9520G>A (p.Val3174Ile) rs199672291
NM_000081.3(LYST):c.9552G>T (p.Leu3184Phe) rs556200563
NM_000081.3(LYST):c.9628-15C>T

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.