ClinVar Miner

List of variants in gene BRAT1 reported as likely benign for not provided

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Gene type:
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Total variants: 36
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HGVS dbSNP
NM_152743.4(BRAT1):c.1032G>A (p.Thr344=) rs371220513
NM_152743.4(BRAT1):c.1135-8C>A rs113613637
NM_152743.4(BRAT1):c.1203T>C (p.Cys401=) rs191610171
NM_152743.4(BRAT1):c.1230T>C (p.Ser410=) rs1583301772
NM_152743.4(BRAT1):c.1396-7G>A rs576174160
NM_152743.4(BRAT1):c.1440C>T (p.Ser480=) rs1583296135
NM_152743.4(BRAT1):c.1470C>T (p.Leu490=) rs1193451009
NM_152743.4(BRAT1):c.1598-9G>T rs754104895
NM_152743.4(BRAT1):c.15C>T (p.Cys5=) rs1485274454
NM_152743.4(BRAT1):c.1635G>A (p.Glu545=) rs770815553
NM_152743.4(BRAT1):c.1638G>A (p.Val546=) rs755145624
NM_152743.4(BRAT1):c.163C>T (p.Leu55=) rs1408897985
NM_152743.4(BRAT1):c.1671T>G (p.Pro557=) rs1583293696
NM_152743.4(BRAT1):c.1734C>T (p.His578=) rs764709405
NM_152743.4(BRAT1):c.1740C>A (p.Pro580=) rs200084998
NM_152743.4(BRAT1):c.1791G>A (p.Leu597=) rs759517314
NM_152743.4(BRAT1):c.1862G>A (p.Arg621Gln) rs138077616
NM_152743.4(BRAT1):c.1867G>A (p.Gly623Ser) rs77015302
NM_152743.4(BRAT1):c.186G>C (p.Val62=) rs754650421
NM_152743.4(BRAT1):c.1893G>A (p.Thr631=) rs775940127
NM_152743.4(BRAT1):c.1911T>G (p.Thr637=) rs1016199390
NM_152743.4(BRAT1):c.1962C>A (p.Gly654=) rs778520339
NM_152743.4(BRAT1):c.2006C>T (p.Pro669Leu) rs570576002
NM_152743.4(BRAT1):c.2040C>T (p.Pro680=) rs1018617325
NM_152743.4(BRAT1):c.2041G>A (p.Glu681Lys) rs145833100
NM_152743.4(BRAT1):c.2088C>T (p.Cys696=) rs369595259
NM_152743.4(BRAT1):c.283-16dup rs759971408
NM_152743.4(BRAT1):c.327C>T (p.Leu109=) rs1438980293
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val) rs140833277
NM_152743.4(BRAT1):c.705C>G (p.Ala235=) rs141151507
NM_152743.4(BRAT1):c.714G>A (p.Val238=) rs1562578908
NM_152743.4(BRAT1):c.729C>T (p.Arg243=) rs770100854
NM_152743.4(BRAT1):c.852G>A (p.Ala284=) rs767671540
NM_152743.4(BRAT1):c.866G>C (p.Cys289Ser) rs140451075
NM_152743.4(BRAT1):c.876C>T (p.Pro292=) rs113279845
NM_152743.4(BRAT1):c.962T>G (p.Leu321Arg) rs150942467

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