Transcript #00027836 (NM_207629.1, ABCG1 gene)

Transcript name ATP-binding cassette, sub-family G (WHITE), member 1, transcript variant 7
Gene name ABCG1 (ATP binding cassette subfamily G member 1)
Chromosome 21
Transcript - NCBI ID NM_207629.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_997512.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-09 05:45:30 +02:00 (CEST)
Date last edited N/A


Variants

962 entries on 10 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-38G>T r.(=) p.(=)
./. c.-32C>T r.(=) p.(=)
./. c.-27T>C r.(=) p.(=)
./. c.-20C>T r.(=) p.(=)
./. c.-18T>G r.(=) p.(=)
./. c.-16C>A r.(=) p.(=)
./. c.-16C>T r.(=) p.(=)
./. c.-16C>G r.(=) p.(=)
./. c.-15C>T r.(=) p.(=)
./. c.-4C>T r.(=) p.(=)
./. c.-3G>A r.(=) p.(=)
./. c.528+34delCinsT r.(=) p.(=)
./. c.596delCinsT r.(?) p.(Thr199Ile)
./. c.1763+43delCinsT r.(=) p.(=)
./. c.1216-49delCinsT r.(=) p.(=)
./. c.1375delGinsA r.(?) p.(Val459Ile)
./. c.11G>A r.(?) p.(Arg4Lys)
./. c.12G>A r.(?) p.(Arg4=)
./. c.12G>C r.(?) p.(Arg4Ser)
./. c.24A>G r.(?) p.(Pro8=)
./. c.32C>T r.(?) p.(Thr11Ile)
./. c.33+1G>A r.spl? p.?
./. c.33+5G>C r.spl? p.?
./. c.33+8C>T r.(=) p.(=)
./. c.33+9G>A r.(=) p.(=)
./. c.33+9G>T r.(=) p.(=)
./. c.33+18C>G r.(=) p.(=)
./. c.33+21T>C r.(=) p.(=)
./. c.33+25T>C r.(=) p.(=)
./. c.33+49T>C r.(=) p.(=)
./. c.34-44A>G r.(=) p.(=)
./. c.34-44_34-43insTGCAGCTTATAACAGGTCTTGT r.(=) p.(=)
./. c.34-36T>G r.(=) p.(=)
./. c.34-36_34-35insATAA r.(=) p.(=)
./. c.34-22T>A r.(=) p.(=)
./. c.34-21T>G r.(=) p.(=)
./. c.34-20G>T r.(=) p.(=)
./. c.34-17T>G r.(=) p.(=)
./. c.34-6T>C r.(=) p.(=)
./. c.36T>C r.(?) p.(Asn12=)
./. c.38C>A r.(?) p.(Ala13Asp)
./. c.39C>T r.(?) p.(Ala13=)
./. c.41G>A r.(?) p.(Ser14Asn)
./. c.42C>A r.(?) p.(Ser14Arg)
./. c.47A>T r.(?) p.(Tyr16Phe)
./. c.51T>C r.(?) p.(Ser17=)
./. c.61A>C r.(?) p.(Thr21Pro)
./. c.62C>T r.(?) p.(Thr21Met)
./. c.62_63insTT r.(?) p.(Glu22TrpfsTer26)
./. c.63G>A r.(?) p.(Thr21=)
./. c.63G>C r.(?) p.(Thr21=)
./. c.64G>C r.(?) p.(Glu22Gln)
./. c.71A>G r.(?) p.(Lys24Arg)
./. c.71A>C r.(?) p.(Lys24Thr)
./. c.74C>T r.(?) p.(Ser25Leu)
./. c.75G>T r.(?) p.(Ser25=)
./. c.75G>A r.(?) p.(Ser25=)
./. c.78G>T r.(?) p.(Val26=)
./. c.78G>A r.(?) p.(Val26=)
./. c.85T>G r.(?) p.(Ser29Ala)
./. c.86C>T r.(?) p.(Ser29Leu)
./. c.87G>A r.(?) p.(Ser29=)
./. c.91G>C r.(?) p.(Asp31His)
./. c.94G>A r.(?) p.(Glu32Lys)
./. c.97G>A r.(?) p.(Val33Met)
./. c.106A>G r.(?) p.(Ser36Gly)
./. c.112A>T r.(?) p.(Met38Leu)
./. c.112A>G r.(?) p.(Met38Val)
./. c.112A>C r.(?) p.(Met38Leu)
./. c.113T>A r.(?) p.(Met38Lys)
./. c.115G>A r.(?) p.(Glu39Lys)
./. c.119C>T r.(?) p.(Ala40Val)
./. c.128C>T r.(?) p.(Thr43Met)
./. c.129G>A r.(?) p.(Thr43=)
./. c.142G>A r.(?) p.(Gly48Arg)
./. c.147T>A r.(?) p.(His49Gln)
./. c.156delA r.(?) p.(Val53Ter)
./. c.158T>A r.(?) p.(Val53Glu)
./. c.162T>A r.(?) p.(Asp54Glu)
./. c.162T>C r.(?) p.(Asp54=)
./. c.171C>G r.(?) p.(Leu57=)
./. c.172A>T r.(?) p.(Thr58Ser)
./. c.173C>T r.(?) p.(Thr58Met)
./. c.174G>A r.(?) p.(Thr58=)
./. c.184C>T r.(?) p.(Arg62Cys)
./. c.184C>G r.(?) p.(Arg62Gly)
./. c.185G>A r.(?) p.(Arg62His)
./. c.189C>A r.(?) p.(Phe63Leu)
./. c.189_191del r.(?) p.(Ser65del)
./. c.192C>T r.(?) p.(Ser64=)
./. c.200C>T r.(?) p.(Pro67Leu)
./. c.202C>T r.(?) p.(Arg68Trp)
./. c.203G>A r.(?) p.(Arg68Gln)
./. c.207G>A r.(?) p.(Arg69=)
./. c.208G>A r.(?) p.(Ala70Thr)
./. c.212C>A r.(?) p.(Ala71Asp)
./. c.215T>G r.(?) p.(Val72Gly)
./. c.226T>C r.(?) p.(Phe76Leu)
./. c.228C>G r.(?) p.(Phe76Leu)
./. c.231G>A r.(?) p.(Arg77=)
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