ClinVar Miner

List of variants in gene SALL1 reported as likely benign by GeneDx

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Total variants: 26
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HGVS dbSNP gnomAD frequency
NM_002968.3(SALL1):c.3535-152C>G rs114061800 0.00855
NM_002968.3(SALL1):c.477C>A (p.Ser159Arg) rs757737676 0.00028
NM_002968.3(SALL1):c.387C>T (p.Ala129=) rs147647889 0.00027
NM_002968.3(SALL1):c.3750C>T (p.Asn1250=) rs142653419 0.00023
NM_002968.3(SALL1):c.3759C>T (p.Ser1253=) rs138153478 0.00016
NM_002968.3(SALL1):c.2373C>A (p.Gly791=) rs377295510 0.00009
NM_002968.3(SALL1):c.1738A>G (p.Ile580Val) rs761575154 0.00008
NM_002968.3(SALL1):c.3330T>C (p.Ser1110=) rs374166565 0.00008
NM_002968.3(SALL1):c.1715C>T (p.Thr572Met) rs373471563 0.00006
NM_002968.3(SALL1):c.351C>T (p.Asn117=) rs145806303 0.00006
NM_002968.3(SALL1):c.1326C>T (p.Ser442=) rs143605364 0.00004
NM_002968.3(SALL1):c.1872C>T (p.Ser624=) rs143548629 0.00004
NM_002968.3(SALL1):c.3771C>T (p.Asn1257=) rs145423593 0.00003
NM_002968.3(SALL1):c.412G>A (p.Gly138Ser) rs756723612 0.00003
NM_002968.3(SALL1):c.130G>A (p.Val44Ile) rs373744120 0.00001
NM_002968.3(SALL1):c.2259C>T (p.Tyr753=) rs1015061989 0.00001
NM_002968.3(SALL1):c.2590G>A (p.Ala864Thr) rs199626036 0.00001
NM_002968.3(SALL1):c.3242T>C (p.Leu1081Ser) rs1241832382 0.00001
NM_002968.3(SALL1):c.3534+5C>T rs775713627 0.00001
NM_002968.3(SALL1):c.*83GCCCC[1] rs374006676
NM_002968.3(SALL1):c.1113ATC[1] (p.Ser375del) rs758101035
NM_002968.3(SALL1):c.1230A>C (p.Gly410=)
NM_002968.3(SALL1):c.448AGC[6] (p.Ser156_Ser159del)
NM_002968.3(SALL1):c.448AGC[7] (p.Ser157_Ser159del) rs113614842
NM_002968.3(SALL1):c.77-54G>A rs79146613
NM_002968.3(SALL1):c.939G>T (p.Val313=) rs1377611548

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