ClinVar Miner

List of variants in gene BRAT1 reported by CeGaT Center for Human Genetics Tuebingen

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Gene type:
ClinVar version:
Total variants: 45
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HGVS dbSNP gnomAD frequency
NM_152743.4(BRAT1):c.962T>G (p.Leu321Arg) rs150942467 0.00675
NM_152743.4(BRAT1):c.866G>C (p.Cys289Ser) rs140451075 0.00598
NM_152743.4(BRAT1):c.2353C>T (p.Arg785Trp) rs61729932 0.00249
NM_152743.4(BRAT1):c.1659C>T (p.Leu553=) rs61746940 0.00205
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616 0.00198
NM_152743.4(BRAT1):c.2208G>T (p.Leu736=) rs61753093 0.00159
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp) rs61753094 0.00152
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val) rs140833277 0.00095
NM_152743.4(BRAT1):c.2041G>A (p.Glu681Lys) rs145833100 0.00079
NM_152743.4(BRAT1):c.1507C>T (p.Pro503Ser) rs147745609 0.00078
NM_152743.4(BRAT1):c.955G>A (p.Val319Ile) rs140903769 0.00034
NM_152743.4(BRAT1):c.1594G>A (p.Gly532Arg) rs142129866 0.00028
NM_152743.4(BRAT1):c.294dup (p.Leu99fs) rs776913277 0.00022
NM_152743.4(BRAT1):c.354C>T (p.Thr118=) rs148913309 0.00014
NM_152743.4(BRAT1):c.1164G>A (p.Ala388=) rs201141165 0.00011
NM_152743.4(BRAT1):c.2009G>A (p.Arg670His) rs147119058 0.00011
NM_152743.4(BRAT1):c.576C>T (p.Pro192=) rs374294371 0.00009
NM_152743.4(BRAT1):c.1340C>T (p.Thr447Met) rs368808380 0.00008
NM_152743.4(BRAT1):c.1791G>A (p.Leu597=) rs759517314 0.00006
NM_152743.4(BRAT1):c.2361G>A (p.Thr787=) rs757243199 0.00004
NM_152743.4(BRAT1):c.1620A>G (p.Ala540=) rs762496445 0.00003
NM_152743.4(BRAT1):c.2148G>A (p.Ala716=) rs756583395 0.00003
NM_152743.4(BRAT1):c.2454C>T (p.Ala818=) rs557088612 0.00003
NM_152743.4(BRAT1):c.474G>A (p.Leu158=) rs141198732 0.00003
NM_152743.4(BRAT1):c.920A>C (p.His307Pro) rs778881636 0.00003
NM_152743.4(BRAT1):c.1522C>T (p.Arg508Cys) rs751548415 0.00002
NM_152743.4(BRAT1):c.2092G>A (p.Val698Met) rs781355172 0.00002
NM_152743.4(BRAT1):c.1129C>T (p.Pro377Ser) rs780327501 0.00001
NM_152743.4(BRAT1):c.1135-4G>A rs1404214519 0.00001
NM_152743.4(BRAT1):c.1280G>A (p.Arg427Gln) rs375466838 0.00001
NM_152743.4(BRAT1):c.158C>G (p.Pro53Arg) rs368397368 0.00001
NM_152743.4(BRAT1):c.2133C>T (p.Cys711=) rs149690979 0.00001
NM_152743.4(BRAT1):c.853C>T (p.Arg285Trp) rs1301692811 0.00001
NM_152743.4(BRAT1):c.113C>T (p.Thr38Met) rs1780250788
NM_152743.4(BRAT1):c.117C>T (p.Val39=)
NM_152743.4(BRAT1):c.1267G>A (p.Val423Ile) rs141807337
NM_152743.4(BRAT1):c.1464T>G (p.Ser488=)
NM_152743.4(BRAT1):c.166G>A (p.Val56Met) rs148548421
NM_152743.4(BRAT1):c.2125_2128del (p.Phe709fs) rs763527391
NM_152743.4(BRAT1):c.2164_2165delinsGA (p.Leu722Asp) rs2128383634
NM_152743.4(BRAT1):c.2169T>A (p.Leu723=) rs150300694
NM_152743.4(BRAT1):c.2283C>G (p.Ala761=)
NM_152743.4(BRAT1):c.2298C>A (p.Asp766Glu) rs144085416
NM_152743.4(BRAT1):c.638dup (p.Val214fs) rs730880324
NM_152743.4(BRAT1):c.983T>C (p.Leu328Pro) rs1291695271

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