Transcript #00009781 (NM_033226.2, ABCC12 gene)

Transcript name ATP-binding cassette, sub-family C (CFTR/MRP), member 12
Gene name ABCC12 (ATP-binding cassette, sub-family C (CFTR/MRP), member 12)
Chromosome 16
Transcript - NCBI ID NM_033226.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_150229.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

121 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.-56C>T -56 r.(=) p.(=) - utr-5 -
./. - c.-56C>T -56 r.(=) p.(=) - utr-5 -
./. - c.-56C>T -56 r.(=) p.(=) - utr-5 -
./. - c.25A>C 25 r.(?) p.(Ile9Leu) - missense -
./. - c.69A>G 69 r.(?) p.(=) - coding-synonymous -
./. - c.69A>G 69 r.(?) p.(=) - coding-synonymous -
./. - c.119+18C>T 119 r.(=) p.(=) - intron 18
./. - c.276-17_276-16del 276 r.(=) p.(=) - intron 16
./. - c.276-17_276-16del 276 r.(=) p.(=) - intron 16
./. - c.276-17_276-16del 276 r.(=) p.(=) - intron 16
./. - c.276-17_276-16del 276 r.(=) p.(=) - intron 16
./. - c.276-17_276-16del 276 r.(=) p.(=) - intron 16
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.305C>A 305 r.(?) p.(Ala102Glu) - missense -
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.657+39C>T 657 r.(=) p.(=) - intron 39
./. - c.1128+24G>C 1128 r.(=) p.(=) - intron 24
./. - c.1128+24G>C 1128 r.(=) p.(=) - intron 24
./. - c.1129-47A>G 1129 r.(=) p.(=) - intron 47
./. - c.1158A>G 1158 r.(?) p.(=) - coding-synonymous -
./. - c.1158A>G 1158 r.(?) p.(=) - coding-synonymous -
./. - c.1158A>G 1158 r.(?) p.(=) - coding-synonymous -
./. - c.1158A>G 1158 r.(?) p.(=) - coding-synonymous -
./. - c.1785+42A>G 1785 r.(=) p.(=) - intron 42
./. - c.1785+42A>G 1785 r.(=) p.(=) - intron 42
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.1848T>C 1848 r.(?) p.(=) - coding-synonymous -
./. - c.2069A>T 2069 r.(?) p.(Glu690Val) - missense -
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2124+38C>A 2124 r.(=) p.(=) - intron 38
./. - c.2352G>A 2352 r.(?) p.(=) - coding-synonymous -
./. - c.2352G>A 2352 r.(?) p.(=) - coding-synonymous -
./. - c.2352G>A 2352 r.(?) p.(=) - coding-synonymous -
./. - c.2352G>A 2352 r.(?) p.(=) - coding-synonymous -
./. - c.2681A>T 2681 r.(?) p.(Lys894Met) - missense -
./. - c.2681A>T 2681 r.(?) p.(Lys894Met) - missense -
./. - c.2681A>T 2681 r.(?) p.(Lys894Met) - missense -
./. - c.2694T>C 2694 r.(?) p.(=) - coding-synonymous -
./. - c.2694T>C 2694 r.(?) p.(=) - coding-synonymous -
./. - c.2694T>C 2694 r.(?) p.(=) - coding-synonymous -
./. - c.2694T>C 2694 r.(?) p.(=) - coding-synonymous -
./. - c.2694T>C 2694 r.(?) p.(=) - coding-synonymous -
./. - c.2965A>T 2965 r.(?) p.(Thr989Ser) - missense -
./. - c.2965A>T 2965 r.(?) p.(Thr989Ser) - missense -
./. - c.2965A>T 2965 r.(?) p.(Thr989Ser) - missense -
./. - c.2965A>T 2965 r.(?) p.(Thr989Ser) - missense -
./. - c.2965A>T 2965 r.(?) p.(Thr989Ser) - missense -
./. - c.2979C>T 2979 r.(?) p.(=) - coding-synonymous -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3037T>C 3037 r.(?) p.(Tyr1013His) - missense-near-splice -
./. - c.3038+41dupC 3038 r.(=) p.(=) - intron 41
./. - c.3038+41dupC 3038 r.(=) p.(=) - intron 41
./. - c.3286-37T>A 3286 r.(=) p.(=) - intron 37
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
./. - c.3349C>T 3349 r.(?) p.(Arg1117Cys) - missense -
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