Transcript #00021243 (NM_000767.4, CYP2B6 gene)

Transcript name cytochrome P450, family 2, subfamily B, polypeptide 6
Gene name CYP2B6 (cytochrome P450, family 2, subfamily B, polypeptide 6)
Chromosome 19
Transcript - NCBI ID NM_000767.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_000758.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

52 entries on 1 page. Showing entries 1 - 52.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-82T>C -82 r.(=) p.(=) - utr-5 -
./. - c.64C>T 64 r.(?) p.(Arg22Cys) - missense -
./. - c.64C>T 64 r.(?) p.(Arg22Cys) - missense -
./. - c.64C>T 64 r.(?) p.(Arg22Cys) - missense -
./. - c.64C>T 64 r.(?) p.(Arg22Cys) - missense -
./. - c.216G>C 216 r.(?) p.(=) - coding-synonymous -
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.485-18C>T 485 r.(=) p.(=) - intron 18
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.516G>T 516 r.(?) p.(Gln172His) - missense -
./. - c.646-17C>T 646 r.(=) p.(=) - intron 17
./. - c.646-17C>T 646 r.(=) p.(=) - intron 17
./. - c.822+44C>T 822 r.(=) p.(=) - intron 44
./. - c.933C>T 933 r.(?) p.(=) - coding-synonymous -
./. - c.966G>C 966 r.(?) p.(Glu322Asp) - missense-near-splice -
./. - c.983T>C 983 r.(?) p.(Ile328Thr) - missense -
./. - c.1153-6C>T 1153 r.(=) p.(=) - splice 6
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.1459C>T 1459 r.(?) p.(Arg487Cys) - missense -
./. - c.*72G>A 1548 r.(=) p.(=) - utr-3 -
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