Transcript #00000027 (NM_000392.3, ABCC2 gene)

Transcript name ATP-binding cassette, sub-family C (CFTR/MRP), member 2
Gene name ABCC2 (ATP-binding cassette, sub-family C (CFTR/MRP), member 2)
Chromosome 10
Transcript - NCBI ID NM_000392.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000383.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2013-10-28 16:42:16 +01:00 (CET)
Date last edited N/A


Variants

148 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.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.-24C>T -24 r.(=) p.(=) - utr-5 -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.116A>T 116 r.(?) p.(Tyr39Phe) - missense -
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.334-49C>T 334 r.(=) p.(=) - intron 49
./. - c.577-20G>A 577 r.(=) p.(=) - intron 20
./. - c.984G>A 984 r.(?) p.(=) - coding-synonymous -
./. - c.1031+31A>C 1031 r.(=) p.(=) - intron 31
./. - c.1058G>A 1058 r.(?) p.(Arg353His) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1249G>A 1249 r.(?) p.(Val417Ile) - missense -
./. - c.1815+27C>G 1815 r.(=) p.(=) - intron 27
./. - c.1900+22T>C 1900 r.(=) p.(=) - intron 22
./. - c.1900+22T>C 1900 r.(=) p.(=) - intron 22
./. - c.1964G>A 1964 r.(?) p.(Arg655Gln) - missense -
./. - c.2362C>T 2362 r.(?) p.(=) - coding-synonymous -
./. - c.2366C>T 2366 r.(?) p.(Ser789Phe) - missense -
./. - c.2546T>G 2546 r.(?) p.(Leu849Arg) - missense -
./. - c.2621-44G>A 2621 r.(=) p.(=) - intron 44
./. - c.2621-44G>A 2621 r.(=) p.(=) - intron 44
./. - c.2621-44G>A 2621 r.(=) p.(=) - intron 44
./. - c.2747+5G>A 2747 r.spl? p.? - splice 5
./. - c.2761G>A 2761 r.(?) p.(Gly921Ser) - missense -
./. - c.2883+11C>T 2883 r.(=) p.(=) - intron 11
./. - c.2883+11C>T 2883 r.(=) p.(=) - intron 11
./. - c.3542G>T 3542 r.(?) p.(Arg1181Leu) - missense -
./. - c.3563T>A 3563 r.(?) p.(Val1188Glu) - missense -
./. - c.3563T>A 3563 r.(?) p.(Val1188Glu) - missense -
./. - c.3563T>A 3563 r.(?) p.(Val1188Glu) - missense -
./. - c.3563T>A 3563 r.(?) p.(Val1188Glu) - missense -
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
./. - c.3742-34T>C 3742 r.(=) p.(=) - intron 34
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