ClinVar Miner

List of variants in gene SMARCAL1 reported as likely benign for not provided

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Gene type:
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Total variants: 16
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HGVS dbSNP
NM_014140.4(SMARCAL1):c.1334+8C>G rs1574453912
NM_014140.4(SMARCAL1):c.1467G>A (p.Val489=) rs145525014
NM_014140.4(SMARCAL1):c.1944C>T (p.Ser648=) rs752241342
NM_014140.4(SMARCAL1):c.2073A>G (p.Lys691=) rs112200018
NM_014140.4(SMARCAL1):c.2141+10C>T rs1574477107
NM_014140.4(SMARCAL1):c.2245-5T>C rs1574484081
NM_014140.4(SMARCAL1):c.2472C>G (p.Thr824=) rs1338342544
NM_014140.4(SMARCAL1):c.2556T>C (p.Val852=) rs1574485907
NM_014140.4(SMARCAL1):c.2754T>C (p.Ser918=) rs1033156954
NM_014140.4(SMARCAL1):c.387T>C (p.Ser129=) rs947471355
NM_014140.4(SMARCAL1):c.426G>A (p.Glu142=) rs767158204
NM_014140.4(SMARCAL1):c.597T>C (p.Pro199=) rs758479373
NM_014140.4(SMARCAL1):c.690C>T (p.Val230=) rs757584821
NM_014140.4(SMARCAL1):c.717A>G (p.Gly239=) rs1574443774
NM_014140.4(SMARCAL1):c.738T>C (p.Asp246=) rs765629645
NM_014140.4(SMARCAL1):c.807T>C (p.Asn269=) rs1574443924

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