ClinVar Miner

List of variants in gene SACS reported as benign for not provided

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Total variants: 23
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HGVS dbSNP
NM_014363.5(SACS):c.10106T>C (p.Val3369Ala) rs17078605
NM_014363.5(SACS):c.10338G>A (p.Gln3446=) rs2737701
NM_014363.5(SACS):c.10611A>G (p.Ala3537=) rs137856939
NM_014363.5(SACS):c.11032C>G (p.Pro3678Ala) rs17078601
NM_014363.5(SACS):c.12304T>C (p.Leu4102=) rs2737699
NM_014363.5(SACS):c.1656A>G (p.Leu552=) rs1536365
NM_014363.5(SACS):c.171+6C>T rs3751368
NM_014363.5(SACS):c.1839G>A (p.Gln613=) rs35840595
NM_014363.5(SACS):c.2146C>T (p.His716Tyr) rs146852400
NM_014363.5(SACS):c.3129A>G (p.Ser1043=) rs148878361
NM_014363.5(SACS):c.3144A>G (p.Val1048=) rs3751369
NM_014363.5(SACS):c.4188C>T (p.His1396=) rs61754477
NM_014363.5(SACS):c.6195T>C (p.Ile2065=) rs4143768
NM_014363.5(SACS):c.6267G>A (p.Ser2089=) rs9550956
NM_014363.5(SACS):c.696T>A (p.Asn232Lys) rs2031640
NM_014363.5(SACS):c.7149C>T (p.Arg2383=) rs17078608
NM_014363.5(SACS):c.810T>G (p.Phe270Leu) rs116907814
NM_014363.5(SACS):c.8127A>C (p.Lys2709Asn) rs78827970
NM_014363.5(SACS):c.8853T>C (p.Val2951=) rs9552929
NM_014363.5(SACS):c.8873A>G (p.Lys2958Arg) rs11839380
NM_014363.5(SACS):c.909A>G (p.Ala303=) rs41315020
NM_014363.5(SACS):c.9846A>G (p.Pro3282=) rs61753111
NM_014363.5(SACS):c.9981T>C (p.Ala3327=) rs2737700

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