Transcript #00000130

Transcript name colon cancer, nonpolyposis type 1 (E. coli), transcript variant 2
Gene name MSH2 (mutS homolog 2)
Chromosome 2
Transcript - NCBI ID NM_001258281.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001245210.1
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.-43C>T r.(=) p.(=)
./. - c.-36C>T r.(=) p.(=)
./. - c.-31+20G>A r.(=) p.(=)
./. - c.-31+78G>C r.(=) p.(=)
./. - c.-30-41A>G r.(=) p.(=)
./. - c.-30-41A>G r.(=) p.(=)
./. - c.13+8C>T r.(=) p.(=)
./. - c.13+29A>G r.(=) p.(=)
./. - c.13+33A>G r.(=) p.(=)
./. - c.13+46T>G r.(=) p.(=)
./. - c.47A>C r.(?) p.(Lys16Thr)
./. - c.75_77del r.(?) p.(Leu28del)
./. - c.75_77del r.(?) p.(Leu28del)
./. - c.75_77del r.(?) p.(Leu28del)
./. - c.76C>G r.(?) p.(Leu26Val)
./. - c.76C>G r.(?) p.(Leu26Val)
./. - c.98G>A r.(?) p.(Arg33Lys)
./. - c.141G>A r.(=) p.(=)
./. - c.141G>A r.(=) p.(=)
./. - c.141G>A r.(=) p.(=)
./. - c.168+28del r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+43G>T r.(=) p.(=)
./. - c.168+47A>G r.(=) p.(=)
./. - c.169-49A>T r.(=) p.(=)
./. - c.169-49A>T r.(=) p.(=)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.237T>G r.(?) p.(Ile79Met)
./. - c.301G>C r.(?) p.(Asp101His)
./. - c.301G>C r.(?) p.(Asp101His)
./. - c.301G>C r.(?) p.(Asp101His)
./. - c.301G>C r.(?) p.(Asp101His)
./. - c.359A>G r.(?) p.(Asn120Ser)
./. - c.359A>G r.(?) p.(Asn120Ser)
./. - c.438A>G r.(=) p.(=)
./. - c.448-46del r.(=) p.(=)
./. - c.448-46del r.(=) p.(=)
./. - c.448-46del r.(=) p.(=)
./. - c.448-46del r.(=) p.(=)
./. - c.448-34C>T r.(=) p.(=)
./. - c.617C>T r.(?) p.(Ala206Val)
./. - c.617C>T r.(?) p.(Ala206Val)
./. - c.617C>T r.(?) p.(Ala206Val)
./. - c.617C>T r.(?) p.(Ala206Val)
./. - c.744+33T>A r.(=) p.(=)
./. - c.767G>T r.(?) p.(Gly256Val)
./. - c.767G>T r.(?) p.(Gly256Val)
./. - c.767G>T r.(?) p.(Gly256Val)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.786C>T r.(=) p.(=)
./. - c.834G>A r.(=) p.(=)
./. - c.834G>A r.(=) p.(=)
./. - c.845A>G r.(?) p.(Gln282Arg)
./. - c.845A>G r.(?) p.(Gln282Arg)
./. - c.845A>G r.(?) p.(Gln282Arg)
./. - c.845A>G r.(?) p.(Gln282Arg)
./. - c.845A>G r.(?) p.(Gln282Arg)
./. - c.847C>G r.(?) p.(Pro283Ala)
./. - c.854T>C r.(?) p.(Met285Thr)
./. - c.878+33A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
./. - c.933A>G r.(=) p.(=)
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