Transcript #00015122 (NM_001142505.1, ABCG4 gene)

Transcript name ATP-binding cassette, sub-family G (WHITE), member 4, transcript variant 2
Gene name ABCG4 (ATP binding cassette subfamily G member 4)
Chromosome 11
Transcript - NCBI ID NM_001142505.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001135977.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 06:09:18 +02:00 (CEST)
Date last edited N/A


Variants

815 entries on 9 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-12-39G>C r.(=) p.(=)
./. c.-12-39G>A r.(=) p.(=)
./. c.-12-34T>C r.(=) p.(=)
./. c.-12-31G>A r.(=) p.(=)
./. c.-12-27C>G r.(=) p.(=)
./. c.-12-23C>A r.(=) p.(=)
./. c.-12-23C>T r.(=) p.(=)
./. c.-12-17A>G r.(=) p.(=)
./. c.-12-14C>T r.(=) p.(=)
./. c.-12-14_-12-9del r.(=) p.(=)
./. c.-12-9C>T r.(=) p.(=)
./. c.-12-8_-12-7insGG r.(=) p.(=)
./. c.-12-7C>G r.(=) p.(=)
./. c.-12-6T>G r.(=) p.(=)
./. c.-12-3_-12-2del r.(=) p.(=)
./. c.-3G>A r.(=) p.(=)
./. c.-2dupT r.(=) p.(=)
./. c.-2T>G r.(=) p.(=)
./. c.811-36delCinsT r.(=) p.(=)
./. c.1437+48delCinsT r.(=) p.(=)
./. c.926-12delCinsG r.(=) p.(=)
./. c.470delCinsT r.(?) p.(Thr157Met)
./. c.540+22delTinsG r.(=) p.(=)
./. c.-12-4delGinsA r.spl? p.?
./. c.2T>C r.(?) p.(Met1?)
./. c.5C>A r.(?) p.(Ala2Glu)
./. c.5C>T r.(?) p.(Ala2Val)
./. c.14C>T r.(?) p.(Ala5Val)
./. c.14C>G r.(?) p.(Ala5Gly)
./. c.15G>T r.(?) p.(Ala5=)
./. c.15G>C r.(?) p.(Ala5=)
./. c.16C>G r.(?) p.(Leu6Val)
./. c.16C>T r.(?) p.(Leu6=)
./. c.24C>T r.(?) p.(Ala8=)
./. c.26T>A r.(?) p.(Val9Glu)
./. c.29G>A r.(?) p.(Gly10Asp)
./. c.36A>T r.(?) p.(Gly12=)
./. c.36A>G r.(?) p.(Gly12=)
./. c.36A>C r.(?) p.(Gly12=)
./. c.39A>G r.(?) p.(Leu13=)
./. c.41G>C r.(?) p.(Gly14Ala)
./. c.43C>T r.(?) p.(Pro15Ser)
./. c.44C>T r.(?) p.(Pro15Leu)
./. c.47G>A r.(?) p.(Gly16Glu)
./. c.49G>T r.(?) p.(Ala17Ser)
./. c.49G>C r.(?) p.(Ala17Pro)
./. c.51T>G r.(?) p.(Ala17=)
./. c.56C>T r.(?) p.(Ala19Val)
./. c.58A>T r.(?) p.(Met20Leu)
./. c.58A>G r.(?) p.(Met20Val)
./. c.63C>T r.(?) p.(Ala21=)
./. c.64G>A r.(?) p.(Val22Met)
./. c.64G>T r.(?) p.(Val22Leu)
./. c.68C>T r.(?) p.(Thr23Met)
./. c.68C>A r.(?) p.(Thr23Lys)
./. c.78C>T r.(?) p.(Asp26=)
./. c.81G>A r.(?) p.(Gly27=)
./. c.84G>A r.(?) p.(Ala28=)
./. c.89C>A r.(?) p.(Pro30His)
./. c.101C>T r.(?) p.(Thr34Ile)
./. c.102C>T r.(?) p.(Thr34=)
./. c.103A>G r.(?) p.(Thr35Ala)
./. c.108C>G r.(?) p.(His36Gln)
./. c.111G>A r.(?) p.(Leu37=)
./. c.114G>A r.(?) p.(Lys38=)
./. c.133A>G r.(?) p.(Thr45Ala)
./. c.139G>A r.(?) p.(Ala47Thr)
./. c.144G>A r.(?) p.(Gln48=)
./. c.146G>A r.(?) p.(Arg49His)
./. c.150C>G r.(?) p.(Phe50Leu)
./. c.156C>T r.(?) p.(His52=)
./. c.164A>G r.(?) p.(Lys55Arg)
./. c.174delC r.(?) p.(Val59TrpfsTer39)
./. c.178G>T r.(?) p.(Asp60Tyr)
./. c.179A>G r.(?) p.(Asp60Gly)
./. c.183C>T r.(?) p.(Ile61=)
./. c.184G>C r.(?) p.(Glu62Gln)
./. c.190G>A r.(?) p.(Val64Met)
./. c.198G>A r.(?) p.(Leu66=)
./. c.207C>T r.(?) p.(Ser69=)
./. c.212G>C r.(?) p.(Arg71Pro)
./. c.217G>A r.(?) p.(Gly73Arg)
./. c.218G>A r.(?) p.(Gly73Glu)
./. c.220C>T r.(?) p.(Pro74Ser)
./. c.225C>T r.(?) p.(Cys75=)
./. c.230G>A r.(?) p.(Arg77His)
./. c.236G>C r.(?) p.(Arg79Thr)
./. c.236G>A r.(?) p.(Arg79Lys)
./. c.237G>C r.(?) p.(Arg79Ser)
./. c.238+9C>T r.(=) p.(=)
./. c.238+12C>A r.(=) p.(=)
./. c.238+24A>T r.(=) p.(=)
./. c.238+28C>T r.(=) p.(=)
./. c.238+35C>T r.(=) p.(=)
./. c.238+35C>G r.(=) p.(=)
./. c.238+36C>G r.(=) p.(=)
./. c.238+46T>G r.(=) p.(=)
./. c.239-41C>T r.(=) p.(=)
./. c.239-40A>T r.(=) p.(=)
./. c.239-34G>T r.(=) p.(=)
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