Transcript #00000129

Transcript name colon cancer, nonpolyposis type 1 (E. coli), transcript variant 1
Gene name MSH2 (mutS homolog 2)
Chromosome 2
Transcript - NCBI ID NM_000251.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000242.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

296 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-29C>T r.(=) p.(=)
./. - c.-22C>T r.(=) p.(=)
./. - c.4G>A r.(?) p.(Ala2Thr)
./. - c.62G>C r.(?) p.(Arg21Pro)
./. - c.128A>G r.(?) p.(Tyr43Cys)
./. - c.128A>G r.(?) p.(Tyr43Cys)
./. - c.211+8C>T r.(=) p.(=)
./. - c.211+29A>G r.(=) p.(=)
./. - c.211+33A>G r.(=) p.(=)
./. - c.211+46T>G r.(=) p.(=)
./. - c.245A>C r.(?) p.(Lys82Thr)
./. - c.273_275del r.(?) p.(Leu94del)
./. - c.273_275del r.(?) p.(Leu94del)
./. - c.273_275del r.(?) p.(Leu94del)
./. - c.274C>G r.(?) p.(Leu92Val)
./. - c.274C>G r.(?) p.(Leu92Val)
./. - c.296G>A r.(?) p.(Arg99Lys)
./. - c.339G>A r.(=) p.(=)
./. - c.339G>A r.(=) p.(=)
./. - c.339G>A r.(=) p.(=)
./. - c.366+28del r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+43G>T r.(=) p.(=)
./. - c.366+47A>G r.(=) p.(=)
./. - c.367-49A>T r.(=) p.(=)
./. - c.367-49A>T r.(=) p.(=)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.435T>G r.(?) p.(Ile145Met)
./. - c.499G>C r.(?) p.(Asp167His)
./. - c.499G>C r.(?) p.(Asp167His)
./. - c.499G>C r.(?) p.(Asp167His)
./. - c.499G>C r.(?) p.(Asp167His)
./. - c.557A>G r.(?) p.(Asn186Ser)
./. - c.557A>G r.(?) p.(Asn186Ser)
./. - c.636A>G r.(=) p.(=)
./. - c.646-46del r.(=) p.(=)
./. - c.646-46del r.(=) p.(=)
./. - c.646-46del r.(=) p.(=)
./. - c.646-46del r.(=) p.(=)
./. - c.646-34C>T r.(=) p.(=)
./. - c.815C>T r.(?) p.(Ala272Val)
./. - c.815C>T r.(?) p.(Ala272Val)
./. - c.815C>T r.(?) p.(Ala272Val)
./. - c.815C>T r.(?) p.(Ala272Val)
./. - c.942+33T>A r.(=) p.(=)
./. - c.965G>T r.(?) p.(Gly322Val)
./. - c.965G>T r.(?) p.(Gly322Val)
./. - c.965G>T r.(?) p.(Gly322Val)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.984C>T r.(=) p.(=)
./. - c.1032G>A r.(=) p.(=)
./. - c.1032G>A r.(=) p.(=)
./. - c.1043A>G r.(?) p.(Gln348Arg)
./. - c.1043A>G r.(?) p.(Gln348Arg)
./. - c.1043A>G r.(?) p.(Gln348Arg)
./. - c.1043A>G r.(?) p.(Gln348Arg)
./. - c.1043A>G r.(?) p.(Gln348Arg)
./. - c.1045C>G r.(?) p.(Pro349Ala)
./. - c.1052T>C r.(?) p.(Met351Thr)
./. - c.1076+33A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
./. - c.1131A>G r.(=) p.(=)
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