Transcript #00017640 (NM_020975.4, RET gene)

Transcript name transcript variant 2
Gene name RET (ret proto-oncogene)
Chromosome 10
Transcript - NCBI ID NM_020975.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_066124.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

305 entries on 4 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? ? c.-37G>C r.(?) p.(=)
?/. - c.47T>C r.(?) p.(Leu16Pro)
-?/. - c.56_58del r.(?) p.(Leu19del)
+?/. - c.95C>T r.(?) p.(Ser32Leu)
-/. - c.135= r.(=) p.(Ala45=)
-?/. - c.135= r.(=) p.(Ala45=)
-/. - 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.166C>A r.(?) p.(Leu56Met)
?/. - c.196T>A r.(?) p.(Phe66Ile)
-?/. - c.200G>A r.(?) p.(Arg67His)
-?/. - c.200G>A r.(?) p.(Arg67His)
+?/. - c.277G>A r.(?) p.(Gly93Ser)
-/. - c.337+9G>A r.(=) p.(=)
-/. - c.337+9G>A r.(=) p.(=)
-/. - c.337+9G>A r.(=) p.(=)
-/. - c.341G>A r.(?) p.(Arg114His)
-/. - c.375C>A r.(?) p.(Val125=)
-/. - c.375C>A r.(?) p.(Val125=)
-/. - c.375C>A r.(?) p.(Val125=)
-/. - c.375C>A r.(?) p.(Val125=)
-?/. - c.405C>T r.(?) p.(=)
?/. - c.448_450del r.(?) p.(Phe150del)
-?/. - c.468C>T r.(?) p.(=)
?/. - c.528T>G r.(?) p.(Ile176Met)
?/. - c.539G>A r.(?) p.(Arg180Gln)
?/. - c.549C>T r.(?) p.(Gly183=)
-?/. - c.597C>T r.(?) p.(Asn199=)
-?/. - c.625+10G>A r.(=) p.(=)
?/. - c.626-72_626-71del r.(=) p.(=)
+?/. - c.626-9G>A r.(=) p.(=)
+?/. - c.692G>A r.(?) p.(Arg231His)
?/. - c.703G>A r.(?) p.(Glu235Lys)
-?/. - c.722C>T r.(?) p.(Ala241Val)
-?/. - c.785T>C r.(?) p.(Val262Ala)
-/. - c.785T>C r.(?) p.(Val262Ala)
-?/. - c.807G>A r.(?) p.(Ala269=)
-/. - c.833C>A r.(?) p.(Thr278Asn)
?/. - c.833C>A r.(?) p.(Thr278Asn)
-?/. - c.833C>A r.(?) p.(Thr278Asn)
+/. - c.874G>A r.(?) p.(Val292Met)
?/. - c.874G>A r.(?) p.(Val292Met)
-?/. - c.907G>A r.(?) p.(Val303Met)
?/. - c.907G>A r.(?) p.(Val303Met)
+/. - c.921del r.(?) p.(Glu309Serfs*3)
-?/. - c.938G>A r.(?) p.(Arg313Gln)
?/? 5 c.938G>A r.(?) p.(Arg313Gln)
+?/. - c.989G>A r.(?) p.(Arg330Gln)
-?/. - c.1008C>T r.(?) p.(=)
-?/. - c.1017G>A r.(?) p.(Ser339=)
-?/. - c.1030G>A r.(?) p.(Gly344Ser)
+?/. - c.1042C>T r.(?) p.(Arg348Trp)
?/? 5i c.1063+9G>A r.(spl?) p.(=)
?/. - c.1083C>A r.(?) p.(Asn361Lys)
?/. - c.1083C>A r.(?) p.(Asn361Lys)
-?/. - c.1118C>T r.(?) p.(Ala373Val)
-?/. - c.1182C>T r.(?) p.(=)
+/. - c.1196C>T r.(?) p.(Pro399Leu)
-/. - c.1264-5C>T r.spl? p.?
-/. - c.1264-5C>T r.spl? p.?
-/. - c.1264-5C>T r.spl? p.?
-/. - c.1264-5C>T r.spl? p.?
?/. - c.1266C>G r.(?) p.(Ile422Met)
-/. - c.1296A>G r.(?) p.(Ala432=)
-/. - c.1296A>G r.(?) p.(Ala432=)
-/. - c.1296A>G r.(?) p.(Ala432=)
-/. - c.1296A>G r.(?) p.(Ala432=)
+/. - c.1372dup r.(1372dup) p.(Ala458GlyfsTer12)
-/. - c.1465G>A r.(?) p.(Asp489Asn)
-?/. - c.1465G>A r.(?) p.(Asp489Asn)
?/. - c.1514A>T r.(?) p.(Glu505Val)
?/. - c.1522+20A>T r.(=) p.(=)
?/. - c.1549C>G r.(?) p.Leu517Val
?/. - c.1591T>A r.(?) p.(Cys531Ser)
-?/. - c.1596C>T r.(?) p.(Gly532=)
?/. - c.1597G>A r.(?) p.(Gly533Ser)
-?/. - c.1648+114G>T r.(?) p.(?)
?/. - c.1666_1668del r.(?) p.(Ser556del)
-?/. - c.1699G>A r.(?) p.(Asp567Asn)
+?/. - c.1699G>A r.(?) p.(Asp567Asn)
-?/. - c.1701C>T r.(?) p.(Asp567=)
+/. - c.1711G>A r.(1711g>a) p.(Asp571Asn)
?/. - c.1727A>C r.(?) p.(Gln576Pro)
+?/. - c.1752C>G r.(?) p.(Asp584Glu)
?/. - c.1756C>T r.(?) p.(Leu586Phe)
?/. - c.1759C>T r.(?) p.(Arg587Trp)
+/. - c.1759+1G>A r.spl? p.?
?/. - c.1799G>A r.(?) p.(Arg600Gln)
?/. - c.1814G>T r.(?) p.(Gly605Val)
+/. - c.1825T>C r.(?) p.(Cys609Arg)
?/? 10 c.1825T>C r.(?) p.(Cys609Arg)
?/? 10 c.1825T>G r.(?) p.(Cys609Gly)
+/. - c.1826G>A r.(?) p.(Cys609Tyr)
?/? 10 c.1826G>A r.(?) p.(Cys609Tyr)
?/? 10 c.1826G>C r.(?) p.(Cys609Ser)
?/? 10 c.1826G>T r.(?) p.(Cys609Phe)
?/? 10 c.1832G>A r.(?) p.(Cys611Tyr)
+/. - c.1832G>A r.(?) p.(Cys611Tyr)
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