Transcript #00015576

Transcript name transcript variant 2
Gene name RAI2 (retinoic acid induced 2)
Chromosome X
Transcript - NCBI ID NM_021785.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_068557.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

51 entries on 1 page. Showing entries 1 - 51.
Legend  

Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-24-26T>G r.(=) p.(=)
?/? c.9C>T r.(=) p.(=)
?/? c.24C>T r.(=) p.(=)
?/? c.105C>T r.(=) p.(=)
?/? c.133C>G r.(?) p.(Leu45Val)
?/? c.166C>G r.(?) p.(Pro56Ala)
?/? c.174T>C r.(=) p.(=)
?/? c.222G>A r.(=) p.(=)
?/? c.300C>T r.(=) p.(=)
?/? c.301G>A r.(?) p.(Ala101Thr)
?/? c.333C>T r.(=) p.(=)
?/? c.337G>A r.(?) p.(Val113Ile)
?/? c.340A>G r.(?) p.(Met114Val)
?/? c.357C>T r.(=) p.(=)
?/? c.369C>T r.(=) p.(=)
?/? c.404A>G r.(?) p.(Asn135Ser)
?/? c.432C>A r.(=) p.(=)
?/? c.433C>T r.(?) p.(Pro145Ser)
?/? c.564C>G r.(=) p.(=)
?/? c.588C>T r.(=) p.(=)
?/? c.699G>A r.(=) p.(=)
?/? c.754A>G N/A N/A
?/? c.773C>T r.(?) p.(Ser258Phe)
?/? c.813C>T r.(=) p.(=)
?/? c.814G>A r.(?) p.(Gly272Ser)
?/? c.864G>A r.(=) p.(=)
?/? c.870C>T r.(=) p.(=)
?/? c.882C>T r.(=) p.(=)
?/? c.917C>T r.(?) p.(Thr306Met)
?/? c.1002C>A r.(=) p.(=)
?/? c.1052G>A r.(?) p.(Arg351Gln)
?/? c.1060G>A r.(?) p.(Glu354Lys)
?/? c.1080G>A r.(=) p.(=)
?/? c.1169C>T r.(?) p.(Thr390Met)
?/? c.1170G>A r.(=) p.(=)
?/? c.1175A>G r.(?) p.(His392Arg)
?/? c.1184C>T r.(?) p.(Pro395Leu)
?/? c.1227C>T r.(=) p.(=)
?/? c.1261G>A r.(?) p.(Glu421Lys)
?/? c.1263A>G r.(=) p.(=)
?/? c.1271C>T r.(?) p.(Ala424Val)
?/? c.1282A>T r.(?) p.(Ile428Phe)
?/? c.1297G>A r.(?) p.(Glu433Lys)
?/? c.1348A>G r.(?) p.(Ile450Val)
?/? c.1409G>C r.(?) p.(Arg470Thr)
?/? c.1420G>A r.(?) p.(Val474Met)
?/? c.1427A>G r.(?) p.(Gln476Arg)
?/? c.1476G>A r.(=) p.(=)
?/? c.1507A>G r.(?) p.(Ile503Val)
?/? c.1537A>G r.(?) p.(Ile513Val)
?/? c.1540C>T r.(?) p.(His514Tyr)
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