ClinVar Miner

List of variants in gene SALL1 reported by PreventionGenetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 22
Download table as spreadsheet
HGVS dbSNP
NM_001127892.1(SALL1):c.3244-44CT[6] rs142249003
NM_002968.2(SALL1):c.129C>T (p.His43=) rs368688611
NM_002968.2(SALL1):c.1904C>T (p.Pro635Leu) rs146454164
NM_002968.2(SALL1):c.2178G>A (p.Arg726=) rs144019351
NM_002968.2(SALL1):c.2310C>T (p.Ile770=) rs61740811
NM_002968.2(SALL1):c.2343G>C (p.Leu781=) rs60270998
NM_002968.2(SALL1):c.2544A>G (p.Gln848=) rs45459896
NM_002968.2(SALL1):c.2574C>T (p.Leu858=) rs1965024
NM_002968.2(SALL1):c.292A>G (p.Met98Val) rs28643388
NM_002968.2(SALL1):c.2967C>T (p.Leu989=) rs759617992
NM_002968.2(SALL1):c.3456C>T (p.His1152=) rs11645288
NM_002968.2(SALL1):c.379G>C (p.Val127Leu) rs138635817
NM_002968.2(SALL1):c.3823G>A (p.Val1275Ile) rs4614723
NM_002968.2(SALL1):c.3872A>G (p.Asn1291Ser) rs74499562
NM_002968.2(SALL1):c.390G>A (p.Pro130=) rs75156807
NM_002968.2(SALL1):c.448_450AGC[11] (p.Ser159dup) rs113614842
NM_002968.2(SALL1):c.448_450AGC[9] (p.Ser159del) rs113614842
NM_002968.2(SALL1):c.472A>G (p.Ser158Gly) rs139646526
NM_002968.2(SALL1):c.475A>G (p.Ser159Gly) rs13336129
NM_002968.2(SALL1):c.478G>A (p.Gly160Ser) rs199760974
NM_002968.2(SALL1):c.478_480GGC[5] (p.Gly163dup) rs1555475414
NM_002968.2(SALL1):c.76+36_76+37delAC rs200502187

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.