Transcript #00000110

Transcript name multiple endocrine neoplasia I, transcript variant 2
Gene name MEN1 (menin 1)
Chromosome 11
Transcript - NCBI ID NM_130799.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_570711.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

83 entries on 1 page. Showing entries 1 - 83.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-22C>A r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-13A>C r.(=) p.(=)
./. - c.-10G>A r.(=) p.(=)
./. - c.-10G>C r.(=) p.(=)
./. - c.-6G>A r.(=) p.(=)
./. - c.30G>T r.(=) p.(=)
./. - c.30G>T r.(=) p.(=)
./. - c.329G>C r.(?) p.(Gly110Ala)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.526G>T r.(?) p.(Ala176Ser)
./. - c.563C>T r.(?) p.(Pro188Leu)
./. - c.563C>T r.(?) p.(Pro188Leu)
./. - c.563C>T r.(?) p.(Pro188Leu)
./. - c.576G>C r.(?) p.(Gln192His)
./. - c.598G>A r.(?) p.(Gly200Ser)
./. - c.681C>T r.(=) p.(=)
./. - c.685C>T r.(?) p.(Arg229Cys)
./. - c.711G>A r.(=) p.(=)
./. - c.740T>C r.(?) p.(Ile247Thr)
./. - c.762G>A r.(=) p.(=)
./. - c.762G>A r.(=) p.(=)
./. - c.763G>A r.(?) p.(Glu255Lys)
./. - c.783+29G>A r.(=) p.(=)
./. - c.784-36G>A r.(=) p.(=)
./. - c.784-36G>A r.(=) p.(=)
./. - c.784-36G>A r.(=) p.(=)
./. - c.784-15_784-14del r.(=) p.(=)
./. - c.784-15_784-14del r.(=) p.(=)
./. - c.784-10C>T r.(=) p.(=)
./. - c.792C>T r.(=) p.(=)
./. - c.1032G>A r.(=) p.(=)
./. - c.1049+43C>T r.(=) p.(=)
./. - c.1049+43C>T r.(=) p.(=)
./. - c.1080C>T r.(=) p.(=)
./. - c.1130A>G r.(?) p.(Lys377Arg)
./. - c.1177C>G r.(?) p.(Gln393Glu)
./. - c.1206C>A r.(=) p.(=)
./. - c.1230C>T r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1296G>A r.(=) p.(=)
./. - c.1395C>T r.(=) p.(=)
./. - c.1428G>C r.(=) p.(=)
./. - c.1478C>T r.(?) p.(Pro493Leu)
./. - c.1541C>G r.(?) p.(Pro514Arg)
./. - c.1826G>C r.(?) p.(Gly609Ala)
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