Transcript #00000089 (NM_000251.1, MSH2 gene)

Transcript name mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli)
Gene name MSH2 (mutS homolog 2, colon cancer, nonpolyposis type 1 (E. coli))
Chromosome 2
Transcript - NCBI ID NM_000251.1
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

119 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. 00 c.-78_-79delGT - -
./. 00 c.(?_-68)-1276+?del - -
./. 00 c.(?_-68)_1076+?del - -
./. 00 c.(?_-68)_1076+?del - -
./. 00 c.(?_-68)_1661+?del - -
./. 00 c.(?_-68)_792+?del - -
./. 01 c.14C>A - p.Pro5Gln
./. 01 c.14C>A - p.Pro5Gln
./. 01 c.21G>C - p.Glu7Asp
./. 01 c.23C>T - p.Thr8Met
./. 01 c.23C>T - p.Thr8Met
./. 01 c.54C>G - p.Gly18Gly
./. 01 c.187dupG - p.Val63GlyfsX19
./. 01 c.211+9C>G - -
./. 01 c.211+9C>G - -
./. 02 c.212-?_1076+?del - -
./. 02 c.295A>C - p.Arg99Arg
./. 02 c.295_296delinsC - p.Arg99GlnfsX75
./. 03 c.505A>G - p.Ile169Val
./. 03 c.513delG - p.Arg171ArgfsX3
./. 03 c.518T>G - p.Leu173Arg
./. 03 c.529G>A - p.Glu177Lys
./. 03 c.597T>C - p.Cys199Arg
./. 03 c.610G>T - p.Gly204X
./. 03 c.610G>T - p.Gly204X
./. 03 c.610G>T - p.Gly204X
./. 03 c.610G>T - p.Gly204X
./. 03 c.616_617insA - p.Thr206AsnfsX26
./. 04 c.646-?_942+?del - -
./. 04 c.646-?_942+?del - -
./. 04 c.736A>T - p.Lys246X
./. 05 c.795T>C - p.Val265Val
./. 05 c.899_890insAT - p.Ile484IlefsX12
./. 05 c.942+3A>T - -
./. 07 c.1077-?_1276+?del - -
./. 07 c.1077-?_1276+?del - -
./. 07 c.1145G>A - p.Arg382His
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1168C>T - p.Leu390Phe
./. 07 c.1216_1219dupCGAC - p.Leu407ProfsX11
./. 07 c.1216_1219dupCGAC - p.Leu407ProfsX11
./. 07 c.1216_1219dupCGAC - p.Leu407ProfsX11
./. 07 c.1221C>G - p.Leu407Leu
./. 07 c.1221C>G - p.Leu407Leu
./. 07 c.1221C>G - p.Leu407Leu
./. 07 c.1223A>G - p.Tyr408Cys
./. 07 c.1223A>G - p.Tyr408Cys
./. 07 c.1225C>A - p.Gln409Lys
./. 07 c.1255C>A - p.Gln419Lys
./. 07 c.1255C>A - p.Gln419Lys
./. 07 c.1255C>A - p.Gln419Lys
./. 07 c.1255C>A - p.Gln419Lys
./. 07 c.1261C>A - p.Leu421Met
./. 07 c.1276+47T>A - -
./. 08 c.1277-1G>A - -
./. 09 c.1387-?_1510+?del - -
./. 09 c.1452_1455delAATG - p.Ile484IlefsX12
./. 09 c.1452_1455delAATG - p.Ile484IlefsX12
./. 09 c.1452_1455delAATG - p.Ile484IlefsX12
./. 10 c.1552_1553delCA - p.Gln518ValfsX10
./. 10 c.1571G>T - p.Arg524Leu
./. 10 c.1661+12G>A - -
./. 10 c.1661+12G>A - -
./. 10 c.1661+12G>A - -
./. 11 c.1662-2A>G - -
./. 11 c.1662-?_1759+?del - -
./. 11 c.1665delA - p.Lys555AsnfsX2
./. 11 c.1688A>C - p.Tyr563Ser
./. 11 c.1688A>C - p.Tyr563Ser
./. 11 c.1690A>G - p.Thr564Ala
./. 11 c.1690A>G - p.Thr564Ala
./. 11 c.1717delG - p.Ala573ProfsX17
./. 11 c.1738G>T - p.Glu580X
./. 11 c.1759_1760insT - p.Gly587ValfsX11
./. 11 c.1759_1760insT - p.Gly587ValfsX11
./. 12 c.1760delG - p.Gly587AlafsX3
./. 12 c.1760-?_2005+?del - -
./. 12 c.1808A>G - p.Asp603Gly
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1886A>G - p.Gln629Arg
./. 12 c.1917T>A - p.His639Gln
./. 12 c.1955C>A - p.Pro652His
./. 13 c.2006-6T>C - -
./. 13 c.2006-6T>C - -
./. 13 c.2006-6T>C - -
./. 13 c.2021_2022delGT - p.Gly674GlufsX23
./. 13 c.2038C>T - p.Arg680X
./. 13 c.2047G>A - p.Gly683Arg
./. 13 c.2064G>A - p.Met688Ile
./. 13 c.2091T>A - p.Cys697X
./. 13 c.2108C>A - p.Ser703Tyr
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