Transcript #00001589

Transcript name transcript variant 1
Gene name BIRC2 (baculoviral IAP repeat containing 2)
Chromosome 11
Transcript - NCBI ID NM_001166.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001157.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

89 entries on 1 page. Showing entries 1 - 89.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-24A>G r.(=) p.(=)
?/? c.-1C>T r.(=) p.(=)
?/? c.26T>G r.(?) p.(Leu9Arg)
?/? c.29T>C r.(?) p.(Phe10Ser)
?/? c.35_41del r.(?) p.(Pro13Ilefs*7)
?/? c.47A>G r.(?) p.(Gln16Arg)
?/? c.101G>A r.(?) p.(Ser34Asn)
?/? c.104A>G r.(?) p.(Asn35Ser)
?/? c.109C>G r.(?) p.(Gln37Glu)
?/? c.163A>G r.(?) p.(Thr55Ala)
?/? c.229G>T r.(?) p.(Val77Leu)
?/? c.245A>G r.(?) p.(Lys82Arg)
?/? c.355G>C r.(?) p.(Ala119Pro)
?/? c.372C>T r.(=) p.(=)
?/? c.400A>G r.(?) p.(Ser134Gly)
?/? c.405T>C r.(=) p.(=)
?/? c.410A>G r.(?) p.(His137Arg)
?/? c.417A>G r.(=) p.(=)
?/? c.473C>G r.(?) p.(Pro158Arg)
?/? c.486T>G r.(?) p.(Asn162Lys)
?/? c.515C>T r.(?) p.(Ser172Leu)
?/? c.525C>T r.(=) p.(=)
?/? c.556G>A r.(?) p.(Ala186Thr)
?/? c.594T>C r.(=) p.(=)
?/? c.704A>T r.(?) p.(Asp235Val)
?/? c.722G>A r.(?) p.(Arg241Gln)
?/? c.813T>G r.(=) p.(=)
?/? c.814C>T r.(?) p.(Arg272*)
?/? c.858G>A r.(=) p.(=)
?/? c.889T>C r.(?) p.(Tyr297His)
?/? c.890A>G r.(?) p.(Tyr297Cys)
?/? c.895+27A>G r.(=) p.(=)
?/? c.895+31T>G r.(=) p.(=)
?/? c.896-40A>T r.(=) p.(=)
?/? c.896-35C>T r.(=) p.(=)
?/? c.896-34G>A r.(=) p.(=)
?/? c.896-16_896-15insT r.(=) p.(=)
?/? c.954T>C r.(=) p.(=)
?/? c.964del r.(?) p.(Pro322Hisfs*3)
?/? c.995+5del r.spl? p.?
?/? c.995+20T>C r.(=) p.(=)
?/? c.995+38T>A r.(=) p.(=)
?/? c.995+50A>G r.(=) p.(=)
?/? c.1021G>A r.(?) p.(Gly341Ser)
?/? c.1074+9A>G r.(=) p.(=)
?/? c.1074+41T>C r.(=) p.(=)
?/? c.1075-29T>C r.(=) p.(=)
?/? c.1123+42T>C r.(=) p.(=)
?/? c.1124-46G>T r.(=) p.(=)
?/? c.1124-23T>A r.(=) p.(=)
?/? c.1124-20G>A r.(=) p.(=)
?/? c.1124-18A>G r.(=) p.(=)
?/? c.1194T>G r.(=) p.(=)
?/? c.1307A>G r.(?) p.(Asn436Ser)
?/? c.1325G>A r.(?) p.(Arg442Lys)
?/? c.1337A>G r.(?) p.(Lys446Arg)
?/? c.1357A>G r.(?) p.(Met453Val)
?/? c.1359G>A r.(?) p.(Met453Ile)
?/? c.1366+13G>T r.(=) p.(=)
?/? c.1366+21C>A r.(=) p.(=)
?/? c.1367-21C>A r.(=) p.(=)
?/? c.1367-15del r.(=) p.(=)
?/? c.1369G>C r.(?) p.(Asp457His)
?/? c.1401T>C r.(=) p.(=)
?/? c.1413A>G r.(=) p.(=)
?/? c.1426C>T r.(?) p.(Leu476Phe)
?/? c.1484T>C r.(?) p.(Ile495Thr)
?/? c.1517C>T r.(?) p.(Ala506Val)
?/? c.1546A>G r.(?) p.(Lys516Glu)
?/? c.1553A>G r.(?) p.(Asn518Ser)
?/? c.1559C>T r.(?) p.(Ala520Val)
?/? c.1584A>G r.(=) p.(=)
?/? c.1621+1G>T r.spl? p.?
?/? c.1621+10T>C r.(=) p.(=)
?/? c.1621+33C>T r.(=) p.(=)
?/? c.1622-39A>G r.(=) p.(=)
?/? c.1645C>T r.(?) p.(Pro549Ser)
?/? c.1654G>T r.(?) p.(Asp552Tyr)
?/? c.1663+39del r.(=) p.(=)
?/? c.1664-42T>C r.(=) p.(=)
?/? c.1664-39A>C r.(=) p.(=)
?/? c.1664-25C>T r.(=) p.(=)
?/? c.1664-4T>C r.spl? p.?
?/? c.1754C>T r.(?) p.(Pro585Leu)
?/? c.1768G>A r.(?) p.(Val590Ile)
?/? c.1822A>G r.(?) p.(Ile608Val)
?/? c.*11T>G r.(=) p.(=)
?/? c.*28A>G r.(=) p.(=)
?/? c.*36G>A r.(=) p.(=)
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