ClinVar Miner

List of variants reported as benign for Amyotrophic lateral sclerosis 21

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Total variants: 46
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HGVS dbSNP
NM_018834.6(MATR3):c.*1076T>C rs2015602
NM_018834.6(MATR3):c.*1087G>C rs116660718
NM_018834.6(MATR3):c.*1259G>C rs62381613
NM_018834.6(MATR3):c.*1278T>C rs116341961
NM_018834.6(MATR3):c.*1288T>G rs10515507
NM_018834.6(MATR3):c.*1394G>A rs572983701
NM_018834.6(MATR3):c.*1425C>G rs145516036
NM_018834.6(MATR3):c.*1482A>T rs79616595
NM_018834.6(MATR3):c.*1535A>G
NM_018834.6(MATR3):c.*1767C>T rs181125183
NM_018834.6(MATR3):c.*177A>G rs13698
NM_018834.6(MATR3):c.*2054T>A
NM_018834.6(MATR3):c.*2174C>T rs775200100
NM_018834.6(MATR3):c.*2194T>A rs760576225
NM_018834.6(MATR3):c.*2200C>T rs770043950
NM_018834.6(MATR3):c.*275C>T rs187985845
NM_018834.6(MATR3):c.*305A>C rs563125595
NM_018834.6(MATR3):c.*313A>G rs180806333
NM_018834.6(MATR3):c.*406A>G rs185734839
NM_018834.6(MATR3):c.*496C>T rs140707719
NM_018834.6(MATR3):c.*640A>G rs145836548
NM_018834.6(MATR3):c.*672G>A rs7305
NM_018834.6(MATR3):c.*708T>C rs14109
NM_018834.6(MATR3):c.*747G>C rs181792838
NM_018834.6(MATR3):c.*769G>A rs561705958
NM_018834.6(MATR3):c.*97C>G rs769044248
NM_018834.6(MATR3):c.-43T>A rs12153162
NM_018834.6(MATR3):c.1130-4A>G
NM_018834.6(MATR3):c.1130-5T>A rs188905656
NM_018834.6(MATR3):c.1132G>A (p.Ala378Thr) rs201075828
NM_018834.6(MATR3):c.1183-5G>A rs369464069
NM_018834.6(MATR3):c.1347C>T (p.Ala449=) rs141986556
NM_018834.6(MATR3):c.1602+6A>G rs80036770
NM_018834.6(MATR3):c.1893C>T (p.Ser631=) rs143527811
NM_018834.6(MATR3):c.2191T>C (p.Leu731=) rs149714542
NM_018834.6(MATR3):c.2271T>C (p.Asp757=) rs753870064
NM_018834.6(MATR3):c.2283C>T (p.Asn761=) rs189752689
NM_018834.6(MATR3):c.2360A>G (p.Asn787Ser) rs148402819
NM_018834.6(MATR3):c.2494-14C>A rs779597861
NM_018834.6(MATR3):c.2504A>G (p.Asn835Ser) rs201165929
NM_018834.6(MATR3):c.2521C>T (p.Arg841Cys) rs781050726
NM_018834.6(MATR3):c.291A>G (p.Leu97=) rs147239107
NM_018834.6(MATR3):c.69G>A (p.Ala23=)
NM_199189.2(MATR3):c.-247C>T rs141402332
NM_199189.2(MATR3):c.-610C>G rs11242456
NM_199189.2(MATR3):c.-643A>G rs765907489

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