Transcript #00020639 (NM_033151.3, ABCC11 gene)

Transcript name transcript variant 2
Gene name ABCC11 (ATP-binding cassette, sub-family C (CFTR/MRP), member 11)
Chromosome 16
Transcript - NCBI ID NM_033151.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_149163.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

194 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.7A>G 7 r.(?) p.(Arg3Gly) - missense -
./. - c.24G>T 24 r.(?) p.(Trp8Cys) - missense -
./. - c.56G>A 56 r.(?) p.(Arg19His) - missense -
./. - c.56G>A 56 r.(?) p.(Arg19His) - missense -
./. - c.56G>A 56 r.(?) p.(Arg19His) - missense -
./. - c.56G>A 56 r.(?) p.(Arg19His) - missense -
./. - c.232C>T 232 r.(?) p.(Pro78Ser) - missense -
./. - c.232C>T 232 r.(?) p.(Pro78Ser) - missense -
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.396-41A>T 396 r.(=) p.(=) - intron 41
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.538G>A 538 r.(?) p.(Gly180Arg) - missense -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.684A>G 684 r.(?) p.(=) - coding-synonymous -
./. - c.777+25T>C 777 r.(=) p.(=) - intron 25
./. - c.777+25T>C 777 r.(=) p.(=) - intron 25
./. - c.777+25T>C 777 r.(=) p.(=) - intron 25
./. - c.777+25T>C 777 r.(=) p.(=) - intron 25
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-49G>T 778 r.(=) p.(=) - intron 49
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-23C>T 778 r.(=) p.(=) - intron 23
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.778-20A>G 778 r.(=) p.(=) - intron 20
./. - c.945A>G 945 r.(?) p.(=) - coding-synonymous -
./. - c.945A>G 945 r.(?) p.(=) - coding-synonymous -
./. - c.945A>G 945 r.(?) p.(=) - coding-synonymous -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.950C>A 950 r.(?) p.(Ala317Glu) - missense-near-splice -
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.951+14C>T 951 r.(=) p.(=) - intron 14
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
./. - c.1122A>G 1122 r.(?) p.(=) - coding-synonymous -
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