Transcript #00015832 (NM_000052.5, ATP7A gene)

Transcript name Manually created transcript. (expired, new version available)
Gene name ATP7A (ATPase, Cu++ transporting, alpha polypeptide)
Chromosome X
Transcript - NCBI ID NM_000052.5
Transcript - Ensembl ID -
Protein - NCBI ID -
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

57 entries on 1 page. Showing entries 1 - 57.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

Position     

RNA change     

Protein     

PolyPhen prediction     

GVS function     

Splice distance     
./. - c.-21-2251C>T -21 r.(=) p.(=) - intron 2251
./. - c.-21-2239C>T -21 r.(=) p.(=) - intron 2239
./. - c.-21-2239C>T -21 r.(=) p.(=) - intron 2239
./. - c.-21-2239C>T -21 r.(=) p.(=) - intron 2239
./. - c.-21-2057C>G -21 r.(=) p.(=) - intron 2057
./. - c.-21-2043G>C -21 r.(=) p.(=) - intron 2043
./. - c.-21-2019C>T -21 r.(=) p.(=) - intron 2019
./. - c.1516A>G 1516 r.(?) p.(Ile506Val) - missense -
./. - c.1768A>G 1768 r.(?) p.(Arg590Gly) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2299G>C 2299 r.(?) p.(Val767Leu) - missense -
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.2782-29C>A 2782 r.(=) p.(=) - intron 29
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.3659-42G>C 3659 r.(=) p.(=) - intron 42
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.4048G>A 4048 r.(?) p.(Glu1350Lys) - missense -
./. - c.*40C>G 4543 r.(=) p.(=) - utr-3 -
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