ClinVar Miner

List of variants in gene SALL1 reported as likely benign

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_001127892.1(SALL1):c.*83_*87GCCCC[1] rs374006676
NM_001127892.1(SALL1):c.157_159AGC[7] (p.Ser60_Ser62del) rs113614842
NM_001127892.1(SALL1):c.187_189GGC[5] (p.Gly66dup) rs1555475414
NM_002968.2(SALL1):c.*1112dup rs551203456
NM_002968.2(SALL1):c.1014T>G (p.Ser338=) rs960886445
NM_002968.2(SALL1):c.129C>T (p.His43=) rs368688611
NM_002968.2(SALL1):c.1322C>A (p.Thr441Asn) rs76275412
NM_002968.2(SALL1):c.1878G>C (p.Glu626Asp) rs80248061
NM_002968.2(SALL1):c.1903C>T (p.Pro635Ser) rs61731136
NM_002968.2(SALL1):c.1904C>T (p.Pro635Leu) rs146454164
NM_002968.2(SALL1):c.1911G>A (p.Ala637=) rs148595195
NM_002968.2(SALL1):c.1950C>T (p.Gly650=) rs138705495
NM_002968.2(SALL1):c.2825C>A (p.Pro942His) rs751069468
NM_002968.2(SALL1):c.2967C>T (p.Leu989=) rs759617992
NM_002968.2(SALL1):c.3120A>G (p.Thr1040=) rs146655918
NM_002968.2(SALL1):c.3180C>A (p.Leu1060=) rs142054182
NM_002968.2(SALL1):c.3199C>T (p.Leu1067Phe) rs1375814966
NM_002968.2(SALL1):c.351C>T (p.Asn117=) rs145806303
NM_002968.2(SALL1):c.3534+5C>T rs775713627
NM_002968.2(SALL1):c.3771C>T (p.Asn1257=) rs145423593
NM_002968.2(SALL1):c.3794G>A (p.Gly1265Glu) rs149302006
NM_002968.2(SALL1):c.379G>C (p.Val127Leu) rs138635817
NM_002968.2(SALL1):c.3872A>G (p.Asn1291Ser) rs74499562
NM_002968.2(SALL1):c.387C>T (p.Ala129=) rs147647889
NM_002968.2(SALL1):c.3915C>T (p.Asn1305=) rs140524372
NM_002968.2(SALL1):c.472A>G (p.Ser158Gly) rs139646526
NM_002968.2(SALL1):c.477_478insAGCGGC (p.Gly160_Gly161insSerGly) rs1555475415
NM_002968.2(SALL1):c.676G>A (p.Val226Ile) rs149603480
NM_002968.2(SALL1):c.809C>T (p.Pro270Leu) rs140827311
NM_002968.2(SALL1):c.855A>G (p.Leu285=) rs762324270
NM_002968.3(SALL1):c.1022T>C (p.Met341Thr) rs1372339294
NM_002968.3(SALL1):c.1485C>T (p.His495=) rs1279763997
NM_002968.3(SALL1):c.2752G>A (p.Ala918Thr) rs144782810
NM_002968.3(SALL1):c.2798_2803dup (p.Asn933_Ser934dup) rs760807997
NM_002968.3(SALL1):c.3084A>G (p.Pro1028=) rs377643763
NM_002968.3(SALL1):c.3322G>A (p.Val1108Ile) rs148931484
NM_002968.3(SALL1):c.3535-44CT[6] rs142249003
NM_002968.3(SALL1):c.3759C>T (p.Ser1253=) rs138153478
NM_002968.3(SALL1):c.3957G>A (p.Lys1319=) rs1366906259
NM_002968.3(SALL1):c.448_450AGC[11] (p.Ser159dup) rs113614842
NM_002968.3(SALL1):c.703G>A (p.Ala235Thr) rs761053549
NM_002968.3(SALL1):c.76+26AC[5] 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.