Transcript #00000186

Transcript name transcript variant 4
Gene name RET (ret proto-oncogene)
Chromosome 10
Transcript - NCBI ID NM_020630.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_065681.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-13G>A r.(=) p.(=)
./. - c.-13G>A r.(=) p.(=)
./. - c.-13G>A r.(=) p.(=)
./. - c.20G>A r.(?) p.(Gly7Asp)
./. - c.20G>C r.(?) p.(Gly7Ala)
./. - c.73+30G>A r.(=) p.(=)
./. - c.74-50G>C r.(=) p.(=)
./. - c.79T>C r.(=) p.(=)
./. - c.166C>A r.(?) p.(Leu56Met)
./. - c.166C>A r.(?) p.(Leu56Met)
./. - c.166C>A r.(?) p.(Leu56Met)
./. - c.166C>A r.(?) p.(Leu56Met)
./. - c.200G>A r.(?) p.(Arg67His)
./. - c.220G>A r.(?) p.(Gly74Ser)
./. - c.224C>T r.(?) p.(Thr75Met)
./. - c.224C>T r.(?) p.(Thr75Met)
./. - c.224C>T r.(?) p.(Thr75Met)
./. - c.304G>A r.(?) p.(Asp102Asn)
./. - c.304G>A r.(?) p.(Asp102Asn)
./. - c.337+34C>T r.(=) p.(=)
./. - c.337+34C>T r.(=) p.(=)
./. - c.337+34C>T r.(=) p.(=)
./. - c.337+41A>C r.(=) p.(=)
./. - c.341G>A r.(?) p.(Arg114His)
./. - c.452A>G r.(?) p.(Asn151Ser)
./. - c.468C>T r.(=) p.(=)
./. - c.597C>T r.(=) p.(=)
./. - c.597C>T r.(=) p.(=)
./. - c.597C>T r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-41G>A r.(=) p.(=)
./. - c.626-21C>T r.(=) p.(=)
./. - c.628G>A r.(?) p.(Glu210Lys)
./. - c.628G>A r.(?) p.(Glu210Lys)
./. - c.731C>T r.(?) p.(Thr244Ile)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.785T>C r.(?) p.(Val262Ala)
./. - c.834C>T r.(=) p.(=)
./. - c.868-9A>G r.(=) p.(=)
./. - c.874G>A r.(?) p.(Val292Met)
./. - c.957C>A r.(=) p.(=)
./. - c.961G>A r.(?) p.(Gly321Arg)
./. - c.1013C>T r.(?) p.(Thr338Ile)
./. - c.1013C>T r.(?) p.(Thr338Ile)
./. - c.1017G>A r.(=) p.(=)
./. - c.1050C>T r.(=) p.(=)
./. - c.1051G>A r.(?) p.(Val351Ile)
./. - c.1063+9G>A r.(=) p.(=)
./. - c.1063+37C>T r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1063+47G>A r.(=) p.(=)
./. - c.1064-22A>G r.(=) p.(=)
./. - c.1095G>A r.(=) p.(=)
./. - c.1118C>T r.(?) p.(Ala373Val)
./. - c.1158G>A r.(=) p.(=)
./. - c.1158G>A r.(=) p.(=)
./. - c.1158G>A r.(=) p.(=)
./. - c.1258G>A r.(?) p.(Ala420Thr)
./. - c.1258G>A r.(?) p.(Ala420Thr)
./. - c.1263+30_1263+37del r.(=) p.(=)
./. - c.1263+47G>C r.(=) p.(=)
./. - c.1264-43C>T r.(=) p.(=)
./. - c.1264-15C>T r.(=) p.(=)
./. - c.1264-15C>T r.(=) p.(=)
./. - c.1264-4C>T r.spl? p.?
./. - c.1264-4C>T r.spl? p.?
./. - c.1266C>T r.(=) p.(=)
./. - c.1308C>T r.(=) p.(=)
./. - c.1311C>T r.(=) p.(=)
./. - c.1386G>A r.(=) p.(=)
./. - c.1432T>C r.(?) p.(Cys478Arg)
./. - c.1465G>A r.(?) p.(Asp489Asn)
./. - c.1465G>A r.(?) p.(Asp489Asn)
./. - c.1530C>T r.(=) p.(=)
./. - c.1573C>G r.(?) p.(Arg525Gly)
./. - c.1574G>A r.(?) p.(Arg525Gln)
./. - c.1597G>T r.(?) p.(Gly533Cys)
./. - c.1648+47C>T r.(=) p.(=)
./. - c.1684A>T r.(?) p.(Thr562Ser)
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