ClinVar Miner

List of variants in gene SALL1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 38
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HGVS dbSNP gnomAD frequency
NM_002968.3(SALL1):c.3872A>G (p.Asn1291Ser) rs74499562 0.01024
NM_002968.3(SALL1):c.1903C>T (p.Pro635Ser) rs61731136 0.00058
NM_002968.3(SALL1):c.129C>T (p.His43=) rs368688611 0.00049
NM_002968.3(SALL1):c.3310C>G (p.Pro1104Ala) rs547153228 0.00048
NM_002968.3(SALL1):c.1322C>A (p.Thr441Asn) rs76275412 0.00034
NM_002968.3(SALL1):c.477C>A (p.Ser159Arg) rs757737676 0.00028
NM_002968.3(SALL1):c.1327G>A (p.Asp443Asn) rs374153597 0.00022
NM_002968.3(SALL1):c.1950C>T (p.Gly650=) rs138705495 0.00019
NM_002968.3(SALL1):c.3603C>T (p.Gly1201=) rs542678985 0.00012
NM_002968.3(SALL1):c.1953C>T (p.Pro651=) rs147169088 0.00007
NM_002968.3(SALL1):c.63C>T (p.Leu21=) rs536125319 0.00006
NM_002968.3(SALL1):c.2565T>G (p.Pro855=) rs778734691 0.00004
NM_002968.3(SALL1):c.2008T>C (p.Phe670Leu) rs565545750 0.00001
NM_002968.3(SALL1):c.220G>A (p.Val74Ile) rs529479120 0.00001
NM_002968.3(SALL1):c.2967C>T (p.Leu989=) rs759617992 0.00001
NM_002968.3(SALL1):c.*9G>A
NM_002968.3(SALL1):c.1143C>T (p.Ser381=)
NM_002968.3(SALL1):c.1527C>T (p.Asn509=)
NM_002968.3(SALL1):c.1992G>A (p.Pro664=)
NM_002968.3(SALL1):c.2121G>A (p.Glu707=)
NM_002968.3(SALL1):c.2397C>T (p.Pro799=)
NM_002968.3(SALL1):c.24G>A (p.Lys8=)
NM_002968.3(SALL1):c.2643A>C (p.Leu881=)
NM_002968.3(SALL1):c.270T>A (p.Pro90=)
NM_002968.3(SALL1):c.2928C>T (p.His976=)
NM_002968.3(SALL1):c.3117C>T (p.Ser1039=)
NM_002968.3(SALL1):c.3322G>C (p.Val1108Leu) rs148931484
NM_002968.3(SALL1):c.3535-44CT[6] rs142249003
NM_002968.3(SALL1):c.3855C>G (p.Leu1285=)
NM_002968.3(SALL1):c.472_475delinsG (p.Ser158_Ser159delinsGly)
NM_002968.3(SALL1):c.478GGC[3] (p.Gly163del)
NM_002968.3(SALL1):c.478GGC[5] (p.Gly163dup) rs1555475414
NM_002968.3(SALL1):c.478GGC[6] (p.Gly163_Ser164insGlyGly)
NM_002968.3(SALL1):c.583G>A (p.Val195Ile)
NM_002968.3(SALL1):c.639A>G (p.Glu213=)
NM_002968.3(SALL1):c.76+26AC[5] rs200502187
NM_002968.3(SALL1):c.787G>T (p.Asp263Tyr)
NM_002968.3(SALL1):c.801T>C (p.Ser267=)

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