ClinVar Miner

List of variants reported as likely benign for Amyotrophic lateral sclerosis 21

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Total variants: 51
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HGVS dbSNP
NM_018834.6(MATR3):c.-56G>A rs59033177
NM_018834.6(MATR3):c.1010A>G (p.His337Arg) rs553687055
NM_018834.6(MATR3):c.1017-4C>T
NM_018834.6(MATR3):c.102G>A (p.Gln34=)
NM_018834.6(MATR3):c.1116A>G (p.Pro372=) rs375938101
NM_018834.6(MATR3):c.1129+7A>G
NM_018834.6(MATR3):c.1129+9A>G rs372039740
NM_018834.6(MATR3):c.1130-9C>T rs760841083
NM_018834.6(MATR3):c.1263A>G (p.Pro421=) rs1581248568
NM_018834.6(MATR3):c.1368C>T (p.Thr456=) rs200027384
NM_018834.6(MATR3):c.1377G>A (p.Ala459=) rs147356202
NM_018834.6(MATR3):c.1401A>G (p.Arg467=) rs774463869
NM_018834.6(MATR3):c.1434+10del
NM_018834.6(MATR3):c.1512G>A (p.Pro504=)
NM_018834.6(MATR3):c.15C>T (p.Phe5=) rs184609870
NM_018834.6(MATR3):c.1603-7T>C
NM_018834.6(MATR3):c.1603-9C>A
NM_018834.6(MATR3):c.1603-9_1603-8del rs1581255414
NM_018834.6(MATR3):c.1689T>C (p.Cys563=)
NM_018834.6(MATR3):c.1778+3A>G rs568895329
NM_018834.6(MATR3):c.1866C>T (p.Thr622=) rs539542619
NM_018834.6(MATR3):c.1879C>G (p.Gln627Glu) rs772231433
NM_018834.6(MATR3):c.1896T>C (p.Gly632=) rs202208841
NM_018834.6(MATR3):c.190T>C (p.Leu64=) rs775134951
NM_018834.6(MATR3):c.1917A>G (p.Thr639=)
NM_018834.6(MATR3):c.1938G>A (p.Gln646=) rs755732018
NM_018834.6(MATR3):c.1947T>C (p.Asn649=) rs777432521
NM_018834.6(MATR3):c.1953T>C (p.Leu651=) rs770765421
NM_018834.6(MATR3):c.1991A>C (p.Glu664Ala) rs139589527
NM_018834.6(MATR3):c.2114G>T (p.Ser705Ile) rs201970174
NM_018834.6(MATR3):c.2148+8_2148+11del rs745750214
NM_018834.6(MATR3):c.2181C>T (p.Asn727=)
NM_018834.6(MATR3):c.2220C>T (p.Asn740=) rs1204915381
NM_018834.6(MATR3):c.2232T>G (p.Gly744=) rs1581261752
NM_018834.6(MATR3):c.2238A>G (p.Glu746=)
NM_018834.6(MATR3):c.2265C>T (p.Asn755=)
NM_018834.6(MATR3):c.2271T>C (p.Asp757=) rs753870064
NM_018834.6(MATR3):c.2318A>C (p.Tyr773Ser) rs368217486
NM_018834.6(MATR3):c.2318A>G (p.Tyr773Cys)
NM_018834.6(MATR3):c.2360A>G (p.Asn787Ser) rs148402819
NM_018834.6(MATR3):c.2454T>C (p.Asn818=)
NM_018834.6(MATR3):c.2460T>C (p.His820=) rs1271177846
NM_018834.6(MATR3):c.2494-6T>A rs376395410
NM_018834.6(MATR3):c.2538A>G (p.Glu846=) rs747688305
NM_018834.6(MATR3):c.2543A>G (p.Ter848=) rs200664940
NM_018834.6(MATR3):c.265A>G (p.Ile89Val) rs528548235
NM_018834.6(MATR3):c.507A>G (p.Pro169=) rs1336473659
NM_018834.6(MATR3):c.531T>C (p.Asp177=)
NM_018834.6(MATR3):c.670T>C (p.Leu224=)
NM_018834.6(MATR3):c.675A>G (p.Arg225=)
NM_018834.6(MATR3):c.732T>C (p.His244=) rs765914696

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