Transcript #00022626 (NM_003786.3, ABCC3 gene)

Transcript name ATP-binding cassette, sub-family C (CFTR/MRP), member 3, transcript variant 1
Gene name ABCC3 (ATP binding cassette subfamily C member 3)
Chromosome 17
Transcript - NCBI ID NM_003786.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_003777.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 21:20:25 +02:00 (CEST)
Date last edited N/A


Variants

2158 entries on 22 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-51C>A r.(=) p.(=)
./. c.-43G>A r.(=) p.(=)
./. c.-35C>A r.(=) p.(=)
./. c.4494delAinsG r.(?) p.(LysGly1498=)
./. c.3954+25delCinsT r.(=) p.(=)
./. c.4509delAinsG r.(?) p.(GluPhe1503=)
./. c.2739delTinsC r.(?) p.(AspGlyGluGlyGln913=)
./. c.1176+19delCinsG r.(=) p.(=)
./. c.654delGinsA r.(?) p.(LeuPhe218=)
./. c.3576delCinsT r.(=) p.(=)
./. c.2340delGinsA r.(?) p.(AlaValAspSerHis780=)
./. c.2350delCinsT r.(?) p.(His784Tyr)
./. c.675-2delAinsC r.spl? p.?
./. c.4114-14delCinsT r.(=) p.(=)
./. c.3033delGinsA r.(?) p.(ArgLeu1011=)
./. c.2445delGinsT r.(?) p.(LeuPro815=)
./. c.1432-47delCinsT r.(=) p.(=)
./. c.1432-28delGinsA r.(=) p.(=)
./. c.1432-18delCinsT r.(=) p.(=)
./. c.879delGinsA r.(?) p.(ArgPro293=)
./. c.509delGinsA r.(?) p.(Arg170His)
./. c.2133delCinsT r.(?) p.(PheGly711=)
./. c.1635+32delTinsA r.(=) p.(=)
./. c.32G>A r.(?) p.(Gly11Asp)
./. c.39G>C r.(?) p.(Lys13Asn)
./. c.46-48A>G r.(=) p.(=)
./. c.46-42T>G r.(=) p.(=)
./. c.46-38G>A r.(=) p.(=)
./. c.46-35C>T r.(=) p.(=)
./. c.46-33G>A r.(=) p.(=)
./. c.46-31C>T r.(=) p.(=)
./. c.46-25A>G r.(=) p.(=)
./. c.46-25A>C r.(=) p.(=)
./. c.46-18T>C r.(=) p.(=)
./. c.46-15_46-14del r.(=) p.(=)
./. c.46-11_46-10insGTGTCCCCAGGACTCC r.(?) p.(Asn18ValfsTer114)
./. c.46-9T>C r.(=) p.(=)
./. c.46-7T>G r.(=) p.(=)
./. c.46-6C>T r.(=) p.(=)
./. c.46-6C>G r.(=) p.(=)
./. c.46-4C>T r.spl? p.?
./. c.62T>C r.(?) p.(Val21Ala)
./. c.62T>G r.(?) p.(Val21Gly)
./. c.66C>T r.(?) p.(His22=)
./. c.68C>G r.(?) p.(Thr23Arg)
./. c.69A>G r.(?) p.(Thr23=)
./. c.77C>T r.(?) p.(Pro26Leu)
./. c.78G>A r.(?) p.(Pro26=)
./. c.79G>A r.(?) p.(Asp27Asn)
./. c.80A>G r.(?) p.(Asp27Gly)
./. c.81C>T r.(?) p.(Asp27=)
./. c.82C>T r.(?) p.(Leu28Phe)
./. c.88C>A r.(?) p.(Pro30Thr)
./. c.89C>T r.(?) p.(Pro30Leu)
./. c.92G>A r.(?) p.(Cys31Tyr)
./. c.100A>G r.(?) p.(Asn34Asp)
./. c.104C>T r.(?) p.(Ser35Phe)
./. c.106C>G r.(?) p.(Leu36Val)
./. c.108G>A r.(?) p.(Leu36=)
./. c.119_120insGCCCTGCATCTACCTGTGGGTC r.(?) p.(Pro50HisfsTer84)
./. c.121C>T r.(?) p.(Pro41Ser)
./. c.128T>C r.(?) p.(Ile43Thr)
./. c.130T>G r.(?) p.(Tyr44Asp)
./. c.135G>T r.(?) p.(Leu45=)
./. c.139G>T r.(?) p.(Val47Phe)
./. c.141C>T r.(?) p.(Val47=)
./. c.142G>A r.(?) p.(Ala48Thr)
./. c.142G>T r.(?) p.(Ala48Ser)
./. c.144C>T r.(?) p.(Ala48=)
./. c.145C>T r.(?) p.(Leu49=)
./. c.152G>A r.(?) p.(Cys51Tyr)
./. c.160C>A r.(?) p.(Leu54Ile)
./. c.166C>A r.(?) p.(Leu56Met)
./. c.166C>G r.(?) p.(Leu56Val)
./. c.169C>T r.(?) p.(Arg57Trp)
./. c.169C>A r.(?) p.(Arg57=)
./. c.170G>A r.(?) p.(Arg57Gln)
./. c.173A>G r.(?) p.(His58Arg)
./. c.174C>T r.(?) p.(His58=)
./. c.176A>G r.(?) p.(His59Arg)
./. c.179G>A r.(?) p.(Cys60Tyr)
./. c.181C>T r.(?) p.(Arg61Cys)
./. c.182G>T r.(?) p.(Arg61Leu)
./. c.182G>A r.(?) p.(Arg61His)
./. c.189C>T r.(?) p.(Tyr63=)
./. c.199_220del r.(?) p.(Ser67TrpfsTer49)
./. c.202C>T r.(?) p.(His68Tyr)
./. c.204C>A r.(?) p.(His68Gln)
./. c.205C>G r.(?) p.(Leu69Val)
./. c.205C>T r.(?) p.(Leu69=)
./. c.206T>C r.(?) p.(Leu69Pro)
./. c.213G>A r.(?) p.(Lys71=)
./. c.214C>G r.(?) p.(Leu72Val)
./. c.221T>A r.(?) p.(Met74Lys)
./. c.222G>A r.(?) p.(Met74Ile)
./. c.222G>T r.(?) p.(Met74Ile)
./. c.222+6T>C r.(=) p.(=)
./. c.222+17T>G r.(=) p.(=)
./. c.222+22T>C r.(=) p.(=)
./. c.222+24C>G r.(=) p.(=)
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