Transcript #00019280

Transcript name transcript variant 2
Gene name THEMIS (thymocyte selection associated)
Chromosome 6
Transcript - NCBI ID NM_001010923.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001010923.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

115 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-8G>C r.(=) p.(=)
?/? c.5C>A r.(?) p.(Ala2Glu)
?/? c.25G>A r.(?) p.(Val9Ile)
?/? c.51A>C r.(=) p.(=)
?/? c.73G>A r.(?) p.(Ala25Thr)
?/? c.91+6C>G r.(=) p.(=)
?/? c.91+34C>T r.(=) p.(=)
?/? c.91+35A>T r.(=) p.(=)
?/? c.91+49T>C r.(=) p.(=)
?/? c.91+50A>G r.(=) p.(=)
?/? c.92-50T>C r.(=) p.(=)
?/? c.98T>C r.(?) p.(Ile33Thr)
?/? c.107T>C r.(?) p.(Met36Thr)
?/? c.136G>A r.(?) p.(Gly46Arg)
?/? c.237T>G r.(=) p.(=)
?/? c.250+10A>T r.(=) p.(=)
?/? c.250+46A>G r.(=) p.(=)
?/? c.251-17C>T r.(=) p.(=)
?/? c.251-16G>A r.(=) p.(=)
?/? c.251-9T>C r.(=) p.(=)
?/? c.288T>C r.(=) p.(=)
?/? c.342T>C r.(=) p.(=)
?/? c.353A>G r.(?) p.(Tyr118Cys)
?/? c.381C>A r.(?) p.(Asn127Lys)
?/? c.384C>T r.(=) p.(=)
?/? c.421G>C r.(?) p.(Val141Leu)
?/? c.431T>C r.(?) p.(Ile144Thr)
?/? c.473A>G r.(?) p.(His158Arg)
?/? c.492T>C r.(=) p.(=)
?/? c.509A>G r.(?) p.(Glu170Gly)
?/? c.522C>T r.(=) p.(=)
?/? c.535G>A r.(?) p.(Glu179Lys)
?/? c.540T>C r.(=) p.(=)
?/? c.590C>A r.(?) p.(Thr197Lys)
?/? c.612T>C r.(=) p.(=)
?/? c.622A>G r.(?) p.(Lys208Glu)
?/? c.656T>A r.(?) p.(Phe219Tyr)
?/? c.693T>A r.(=) p.(=)
?/? c.709+9C>G r.(=) p.(=)
?/? c.709+10C>A r.(=) p.(=)
?/? c.709+12C>G r.(=) p.(=)
?/? c.709+21A>C r.(=) p.(=)
?/? c.709+31A>T r.(=) p.(=)
?/? c.709+38G>A r.(=) p.(=)
?/? c.709+47G>T r.(=) p.(=)
?/? c.724A>G r.(?) p.(Ile242Val)
?/? c.728G>A r.(?) p.(Arg243His)
?/? c.739A>G r.(?) p.(Ser247Gly)
?/? c.751G>C r.(?) p.(Glu251Gln)
?/? c.754G>A r.(?) p.(Val252Ile)
?/? c.785A>G r.(?) p.(Asn262Ser)
?/? c.801G>A r.(=) p.(=)
?/? c.846C>T r.(=) p.(=)
?/? c.878G>A r.(?) p.(Gly293Glu)
?/? c.923T>A r.(?) p.(Val308Glu)
?/? c.953T>C r.(?) p.(Ile318Thr)
?/? c.1038G>A r.(=) p.(=)
?/? c.1071C>A r.(=) p.(=)
?/? c.1086G>A r.(=) p.(=)
?/? c.1101G>C r.(=) p.(=)
?/? c.1114G>A r.(?) p.(Ala372Thr)
?/? c.1115C>A r.(?) p.(Ala372Glu)
?/? c.1124C>A r.(?) p.(Ser375Tyr)
?/? c.1190C>T r.(?) p.(Thr397Ile)
?/? c.1229T>A r.(?) p.(Val410Asp)
?/? c.1245dup r.(?) p.(Ile416Asnfs*7)
?/? c.1245_1246del r.(?) p.(Lys415Asnfs*7)
?/? c.1270G>A r.(?) p.(Ala424Thr)
?/? c.1308G>A r.(=) p.(=)
?/? c.1332C>T r.(=) p.(=)
?/? c.1369T>G r.(?) p.(Phe457Val)
?/? c.1371C>T r.(=) p.(=)
?/? c.1375G>A r.(?) p.(Val459Met)
?/? c.1380G>C r.(?) p.(Lys460Asn)
?/? c.1400C>T r.(?) p.(Ser467Phe)
?/? c.1410G>A r.(=) p.(=)
?/? c.1472T>A r.(?) p.(Leu491His)
?/? c.1529A>C r.(?) p.(Asn510Thr)
?/? c.1549A>G r.(?) p.(Ser517Gly)
?/? c.1559C>G r.(?) p.(Ser520Cys)
?/? c.1592T>C r.(?) p.(Leu531Pro)
?/? c.1593G>A r.(=) p.(=)
?/? c.1599A>G r.(=) p.(=)
?/? c.1600G>C r.(?) p.(Glu534Gln)
?/? c.1673C>T r.(?) p.(Pro558Leu)
?/? c.1722A>G r.(=) p.(=)
?/? c.1733C>T r.(?) p.(Thr578Met)
?/? c.1737A>G r.(=) p.(=)
?/? c.1751C>T r.(?) p.(Ser584Phe)
?/? c.1758+23T>C r.(=) p.(=)
?/? c.1758+27C>T r.(=) p.(=)
?/? c.1758+44T>G r.(=) p.(=)
?/? c.1759-8C>A r.(=) p.(=)
?/? c.1767C>T r.(=) p.(=)
?/? c.1779C>G r.(=) p.(=)
?/? c.1790A>G r.(?) p.(His597Arg)
?/? c.1802C>T r.(?) p.(Ala601Val)
?/? c.1810G>A r.(?) p.(Asp604Asn)
?/? c.1828G>A r.(?) p.(Gly610Ser)
?/? c.1829G>A r.(?) p.(Gly610Asp)
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