ClinVar Miner

List of variants in gene RSAD2

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Total variants: 37
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HGVS dbSNP gnomAD frequency
NM_080657.5(RSAD2):c.12T>C (p.Leu4=) rs35784105 0.01643
NM_080657.5(RSAD2):c.125T>G (p.Leu42Arg) rs17851586 0.01460
NM_080657.5(RSAD2):c.420G>A (p.Val140=) rs116498125 0.00758
NM_080657.5(RSAD2):c.90G>A (p.Pro30=) rs2305256 0.00285
NM_080657.5(RSAD2):c.649G>A (p.Ala217Thr) rs140690041 0.00018
NM_080657.5(RSAD2):c.521A>G (p.Asp174Gly) rs373866214 0.00007
NM_080657.5(RSAD2):c.626G>A (p.Arg209Lys) rs769334243 0.00005
NM_080657.5(RSAD2):c.512A>G (p.Glu171Gly) rs369027364 0.00004
NM_080657.5(RSAD2):c.530C>T (p.Ala177Val) rs1040483187 0.00003
NM_080657.5(RSAD2):c.242G>A (p.Arg81His) rs751694276 0.00002
NM_080657.5(RSAD2):c.785C>T (p.Ala262Val) rs201649824 0.00002
NM_080657.5(RSAD2):c.572T>C (p.Ile191Thr) rs781571900 0.00001
NM_080657.5(RSAD2):c.724C>T (p.Pro242Ser) rs769680787 0.00001
NM_080657.5(RSAD2):c.959C>T (p.Pro320Leu) rs1663762557 0.00001
NM_080657.5(RSAD2):c.1051A>G (p.Ile351Val) rs772284239
NM_080657.5(RSAD2):c.183G>T (p.Glu61Asp)
NM_080657.5(RSAD2):c.185A>G (p.Glu62Gly)
NM_080657.5(RSAD2):c.19G>C (p.Ala7Pro)
NM_080657.5(RSAD2):c.209C>A (p.Thr70Asn)
NM_080657.5(RSAD2):c.214C>A (p.Pro72Thr)
NM_080657.5(RSAD2):c.227A>G (p.Asn76Ser) rs2527812099
NM_080657.5(RSAD2):c.352G>C (p.Glu118Gln) rs201282882
NM_080657.5(RSAD2):c.514T>C (p.Tyr172His)
NM_080657.5(RSAD2):c.532A>G (p.Ile178Val) rs554141538
NM_080657.5(RSAD2):c.533T>A (p.Ile178Asn)
NM_080657.5(RSAD2):c.553G>A (p.Glu185Lys)
NM_080657.5(RSAD2):c.603G>A (p.Val201=) rs1663535417
NM_080657.5(RSAD2):c.64A>C (p.Ser22Arg)
NM_080657.5(RSAD2):c.697A>G (p.Met233Val)
NM_080657.5(RSAD2):c.711C>G (p.Ile237Met) rs143741204
NM_080657.5(RSAD2):c.751C>T (p.Leu251Phe)
NM_080657.5(RSAD2):c.769A>T (p.Asn257Tyr) rs1316561135
NM_080657.5(RSAD2):c.778G>A (p.Glu260Lys)
NM_080657.5(RSAD2):c.818A>G (p.Asp273Gly) rs758663261
NM_080657.5(RSAD2):c.835T>C (p.Phe279Leu) rs1444911500
NM_080657.5(RSAD2):c.863G>C (p.Cys288Ser)
NM_080657.5(RSAD2):c.899C>T (p.Ser300Phe)

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