Transcript #00002627 (NM_001136018.2, EPHX1 gene)

Transcript name transcript variant 2
Gene name EPHX1 (epoxide hydrolase 1, microsomal (xenobiotic))
Chromosome 1
Transcript - NCBI ID NM_001136018.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001129490.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-29 14:03:46 +01:00 (CET)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-45G>A -5 r.(=) p.(=) - intron 45
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.-5-29G>A -5 r.(=) p.(=) - intron 29
./. - c.145C>T 145 r.(?) p.(Arg49Cys) - missense -
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.183+20G>A 183 r.(=) p.(=) - intron 20
./. - c.212G>A 212 r.(?) p.(Arg71His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.337T>C 337 r.(?) p.(Tyr113His) - missense -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.357G>A 357 r.(?) p.(=) - coding-synonymous -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.416A>G 416 r.(?) p.(His139Arg) - missense -
./. - c.592+34G>A 592 r.(=) p.(=) - intron 34
./. - c.592+34G>A 592 r.(=) p.(=) - intron 34
./. - c.592+34G>A 592 r.(=) p.(=) - intron 34
./. - c.722+18G>A 722 r.(=) p.(=) - intron 18
./. - c.741C>T 741 r.(?) p.(=) - coding-synonymous -
./. - c.741C>T 741 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.852C>T 852 r.(?) p.(=) - coding-synonymous -
./. - c.932-12G>A 932 r.(=) p.(=) - intron 12
./. - c.1041-42delC 1041 r.(=) p.(=) - intron 42
./. - c.1041-42delC 1041 r.(=) p.(=) - intron 42
./. - c.1041-42delC 1041 r.(=) p.(=) - intron 42
./. - c.1041-38_1041-35del 1041 r.(=) p.(=) - intron 35
./. - c.1071C>T 1071 r.(?) p.(=) - coding-synonymous -
./. - c.1071C>T 1071 r.(?) p.(=) - coding-synonymous -
./. - c.1071C>T 1071 r.(?) p.(=) - coding-synonymous -
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