ClinVar Miner

List of variants in gene SALL4 reported by PreventionGenetics, part of Exact Sciences

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Total variants: 50
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HGVS dbSNP gnomAD frequency
NM_020436.5(SALL4):c.540T>C (p.Asn180=) rs6013281 0.99661
NM_020436.5(SALL4):c.1860A>G (p.Thr620=) rs6021437 0.31314
NM_020436.5(SALL4):c.1056G>A (p.Ala352=) rs13038893 0.29998
NM_020436.5(SALL4):c.1520T>G (p.Leu507Arg) rs6126344 0.29053
NM_020436.5(SALL4):c.2640G>C (p.Ser880=) rs17802735 0.09099
NM_020436.5(SALL4):c.2392A>C (p.Ile798Leu) rs6091375 0.08032
NM_020436.5(SALL4):c.2037C>T (p.Thr679=) rs13043248 0.07305
NM_020436.5(SALL4):c.645C>G (p.Leu215=) rs61737139 0.02226
NM_020436.5(SALL4):c.2215G>T (p.Ala739Ser) rs41274696 0.00290
NM_020436.5(SALL4):c.2483C>T (p.Thr828Met) rs147158259 0.00206
NM_020436.5(SALL4):c.1950C>T (p.Gly650=) rs149008635 0.00121
NM_020436.5(SALL4):c.2166A>G (p.Leu722=) rs141708963 0.00110
NM_020436.5(SALL4):c.1287T>G (p.Phe429Leu) rs143818932 0.00106
NM_020436.5(SALL4):c.2041G>A (p.Ala681Thr) rs147385529 0.00056
NM_020436.5(SALL4):c.541G>A (p.Val181Met) rs139382539 0.00052
NM_020436.5(SALL4):c.2268C>T (p.Ser756=) rs145078336 0.00044
NM_020436.5(SALL4):c.2162C>T (p.Thr721Met) rs147195029 0.00041
NM_020436.5(SALL4):c.1391C>T (p.Pro464Leu) rs139485493 0.00031
NM_020436.5(SALL4):c.1630C>T (p.Pro544Ser) rs150402866 0.00031
NM_020436.5(SALL4):c.3103G>A (p.Gly1035Ser) rs76648342 0.00030
NM_020436.5(SALL4):c.1113C>G (p.Val371=) rs77810153 0.00023
NM_020436.5(SALL4):c.2028C>T (p.Asn676=) rs755057820 0.00006
NM_020436.5(SALL4):c.766A>G (p.Thr256Ala) rs139802240 0.00003
NM_020436.5(SALL4):c.1567G>C (p.Gly523Arg) rs113920122 0.00001
NM_020436.5(SALL4):c.536C>G (p.Thr179Ser) rs201303046 0.00001
NM_020436.5(SALL4):c.990C>T (p.Leu330=) rs758094968 0.00001
NM_020436.5(SALL4):c.1023G>A (p.Ser341=)
NM_020436.5(SALL4):c.1162A>T (p.Ser388Cys)
NM_020436.5(SALL4):c.1217G>A (p.Gly406Glu)
NM_020436.5(SALL4):c.1242_1245del (p.Cys415fs)
NM_020436.5(SALL4):c.1379_1380del (p.Ser460fs)
NM_020436.5(SALL4):c.1472C>T (p.Ser491Leu)
NM_020436.5(SALL4):c.167C>T (p.Ala56Val)
NM_020436.5(SALL4):c.2400delinsTT (p.Ser800_Lys801insTer)
NM_020436.5(SALL4):c.2461+6A>G
NM_020436.5(SALL4):c.2477C>G (p.Pro826Arg)
NM_020436.5(SALL4):c.2594G>T (p.Arg865Leu)
NM_020436.5(SALL4):c.2743-3T>C
NM_020436.5(SALL4):c.2788_2789delinsC (p.Gly930fs)
NM_020436.5(SALL4):c.2831C>T (p.Thr944Met)
NM_020436.5(SALL4):c.2916C>T (p.Tyr972=)
NM_020436.5(SALL4):c.3098C>T (p.Thr1033Ile)
NM_020436.5(SALL4):c.339A>G (p.Glu113=)
NM_020436.5(SALL4):c.411C>G (p.Gly137=) rs201560082
NM_020436.5(SALL4):c.454G>A (p.Val152Met)
NM_020436.5(SALL4):c.534C>G (p.Asn178Lys)
NM_020436.5(SALL4):c.67C>T (p.Pro23Ser)
NM_020436.5(SALL4):c.789C>T (p.His263=)
NM_020436.5(SALL4):c.888C>A (p.His296Gln)
NM_020436.5(SALL4):c.962G>A (p.Arg321Gln)

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