Transcript #00021663

Transcript name zinc finger protein 491
Gene name ZNF491 (zinc finger protein 491)
Chromosome 19
Transcript - NCBI ID NM_152356.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_689569.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

72 entries on 1 page. Showing entries 1 - 72.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-7-44G>A r.(=) p.(=)
?/? c.-7-13G>A r.(=) p.(=)
?/? c.31G>A r.(?) p.(Gly11Ser)
?/? c.36T>C r.(=) p.(=)
?/? c.60G>C r.(?) p.(Gln20His)
?/? c.62del r.(?) p.(Pro22Argfs*5)
?/? c.65C>T r.(?) p.(Pro22Leu)
?/? c.66G>A r.(=) p.(=)
?/? c.122C>T r.(?) p.(Thr41Ile)
?/? c.130G>A r.(?) p.(Glu44Lys)
?/? c.146A>G r.(?) p.(Tyr49Cys)
?/? c.149C>T r.(?) p.(Ser50Leu)
?/? c.194A>G r.(?) p.(His65Arg)
?/? c.219G>C r.(?) p.(Lys73Asn)
?/? c.220C>T r.(?) p.(Pro74Ser)
?/? c.239G>A r.(?) p.(Arg80His)
?/? c.252G>A r.(=) p.(=)
?/? c.289C>T r.(?) p.(His97Tyr)
?/? c.292A>C r.(?) p.(Thr98Pro)
?/? c.304C>T r.(?) p.(Pro102Ser)
?/? c.325G>C r.(?) p.(Glu109Gln)
?/? c.341C>A r.(?) p.(Ser114Tyr)
?/? c.355C>T r.(?) p.(Arg119*)
?/? c.356G>A r.(?) p.(Arg119Gln)
?/? c.362A>G r.(?) p.(Tyr121Cys)
?/? c.365T>C r.(?) p.(Met122Thr)
?/? c.371C>T r.(?) p.(Thr124Met)
?/? c.398G>C r.(?) p.(Cys133Ser)
?/? c.407G>T r.(?) p.(Cys136Phe)
?/? c.432T>A r.(?) p.(Ser144Arg)
?/? c.451C>T r.(?) p.(Arg151*)
?/? c.472C>T r.(?) p.(Arg158*)
?/? c.473G>A r.(?) p.(Arg158Gln)
?/? c.475T>C r.(?) p.(Tyr159His)
?/? c.490T>C r.(?) p.(Cys164Arg)
?/? c.507T>A r.(?) p.(Ser169Arg)
?/? c.524G>C r.(?) p.(Arg175Pro)
?/? c.559T>C r.(?) p.(Tyr187His)
?/? c.605T>G r.(?) p.(Phe202Cys)
?/? c.641C>T r.(?) p.(Pro214Leu)
?/? c.642G>A r.(=) p.(=)
?/? c.674A>G r.(?) p.(Asn225Ser)
?/? c.683G>A r.(?) p.(Ser228Asn)
?/? c.695G>T r.(?) p.(Arg232Met)
?/? c.728A>G r.(?) p.(Tyr243Cys)
?/? c.751G>A r.(?) p.(Ala251Thr)
?/? c.757T>C r.(?) p.(Ser253Pro)
?/? c.764T>G r.(?) p.(Leu255Arg)
?/? c.766A>G r.(?) p.(Ile256Val)
?/? c.775C>G r.(?) p.(Arg259Gly)
?/? c.869A>C r.(?) p.(Glu290Ala)
?/? c.906G>A r.(=) p.(=)
?/? c.926C>T r.(?) p.(Thr309Ile)
?/? c.939G>A r.(=) p.(=)
?/? c.978C>T r.(=) p.(=)
?/? c.998G>C r.(?) p.(Gly333Ala)
?/? c.1027C>A r.(=) p.(=)
?/? c.1044T>G r.(=) p.(=)
?/? c.1062C>G r.(=) p.(=)
?/? c.1067A>T r.(?) p.(Glu356Val)
?/? c.1102A>C r.(?) p.(Ser368Arg)
?/? c.1118A>G r.(?) p.(His373Arg)
?/? c.1132G>A r.(?) p.(Ala378Thr)
?/? c.1154G>A r.(?) p.(Cys385Tyr)
?/? c.1171G>C r.(?) p.(Ala391Pro)
?/? c.1190A>G r.(?) p.(Tyr397Cys)
?/? c.1196G>T r.(?) p.(Arg399Ile)
?/? c.1202A>G r.(?) p.(His401Arg)
?/? c.1223A>G r.(?) p.(Glu408Gly)
?/? c.1277G>A r.(?) p.(Cys426Tyr)
?/? c.1280G>A r.(?) p.(Arg427Gln)
?/? c.*12del r.(=) p.(=)
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