ClinVar Miner

List of variants in gene SALL1 reported as likely benign for abdominal and pelvic region disorder

Included ClinVar conditions (913):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 37
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HGVS dbSNP
NM_002968.2(SALL1):c.*1112dup rs551203456
NM_002968.2(SALL1):c.*192T>C rs3743767
NM_002968.2(SALL1):c.*437C>A rs371127619
NM_002968.2(SALL1):c.*550G>T rs377665001
NM_002968.2(SALL1):c.*646C>T rs143159240
NM_002968.2(SALL1):c.*83_*87GCCCC[1] rs374006676
NM_002968.2(SALL1):c.*922T>G rs184690178
NM_002968.2(SALL1):c.1006G>A (p.Gly336Ser) rs776766459
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.1731C>G (p.Pro577=) rs767216757
NM_002968.2(SALL1):c.1904C>T (p.Pro635Leu) rs146454164
NM_002968.2(SALL1):c.2008T>C (p.Phe670Leu) rs565545750
NM_002968.2(SALL1):c.2178G>A (p.Arg726=) rs144019351
NM_002968.2(SALL1):c.220G>A (p.Val74Ile) rs529479120
NM_002968.2(SALL1):c.2544A>G (p.Gln848=) rs45459896
NM_002968.2(SALL1):c.263G>A (p.Ser88Asn) rs760971365
NM_002968.2(SALL1):c.3120A>G (p.Thr1040=) rs146655918
NM_002968.2(SALL1):c.3199C>T (p.Leu1067Phe) rs1375814966
NM_002968.2(SALL1):c.3222G>A (p.Ala1074=) rs61731131
NM_002968.2(SALL1):c.3711T>C (p.Tyr1237=) rs3743768
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.389C>T (p.Pro130Leu) rs576713482
NM_002968.2(SALL1):c.390G>A (p.Pro130=) rs75156807
NM_002968.2(SALL1):c.3915C>T (p.Asn1305=) rs140524372
NM_002968.2(SALL1):c.3942C>T (p.Phe1314=) rs189411650
NM_002968.2(SALL1):c.448_450AGC[7] (p.Ser157_Ser159del) rs113614842
NM_002968.2(SALL1):c.472A>G (p.Ser158Gly) rs139646526
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.537C>T (p.Leu179=) rs200539812
NM_002968.2(SALL1):c.676G>A (p.Val226Ile) rs149603480
NM_002968.2(SALL1):c.76+10C>G rs758439424
NM_002968.2(SALL1):c.855A>G (p.Leu285=) rs762324270

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