Transcript #00000055

Transcript name ATP-binding cassette, sub-family B (MDR/TAP), member 10
Gene name ABCB10 (ATP-binding cassette, sub-family B (MDR/TAP), member 10)
Chromosome 1
Transcript - NCBI ID NM_012089.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_036221.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

105 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.517+28C>G r.(=) p.(=)
?/? c.518-40C>T r.(=) p.(=)
?/? c.518-30C>A r.(=) p.(=)
?/? c.518-23T>C r.(=) p.(=)
?/? c.537G>A r.(=) p.(=)
?/? c.552C>T r.(=) p.(=)
?/? c.555C>T r.(=) p.(=)
?/? c.615G>A r.(=) p.(=)
?/? c.626A>G r.(?) p.(Asp209Gly)
?/? c.637C>T r.(?) p.(Arg213Cys)
?/? c.638G>A r.(?) p.(Arg213His)
?/? c.652C>T r.(?) p.(Leu218Phe)
?/? c.718+5C>T r.spl? p.?
?/? c.718+13C>T r.(=) p.(=)
?/? c.718+42A>T r.(=) p.(=)
?/? c.718+44A>G r.(=) p.(=)
?/? c.718+45T>C r.(=) p.(=)
?/? c.718+52T>A r.(=) p.(=)
?/? c.727A>G r.(?) p.(Ile243Val)
?/? c.787T>C r.(?) p.(Phe263Leu)
?/? c.800G>A r.(?) p.(Arg267His)
?/? c.888C>T r.(=) p.(=)
?/? c.898G>C r.(?) p.(Ala300Pro)
?/? c.903C>T r.(=) p.(=)
?/? c.904G>A r.(?) p.(Val302Ile)
?/? c.920T>C r.(?) p.(Met307Thr)
?/? c.922-28C>T r.(=) p.(=)
?/? c.979A>G r.(?) p.(Ile327Val)
?/? c.1001G>A r.(?) p.(Arg334Gln)
?/? c.1008A>G r.(=) p.(=)
?/? c.1010G>A r.(?) p.(Arg337Gln)
?/? c.1022A>C r.(?) p.(Lys341Thr)
?/? c.1056+21G>A r.(=) p.(=)
?/? c.1056+43G>A r.(=) p.(=)
?/? c.1057-32C>T r.(=) p.(=)
?/? c.1152A>T r.(=) p.(=)
?/? c.1180G>A r.(?) p.(Ala394Thr)
?/? c.1183C>T r.(?) p.(Arg395Trp)
?/? c.1203A>T r.(=) p.(=)
?/? c.1203+33G>A r.(=) p.(=)
?/? c.1204-5G>A r.spl? p.?
?/? c.1254G>C r.(=) p.(=)
?/? c.1270G>C r.(?) p.(Ala424Pro)
?/? c.1277T>G r.(?) p.(Met426Arg)
?/? c.1281C>T r.(=) p.(=)
?/? c.1306A>G r.(?) p.(Met436Val)
?/? c.1339+51C>T r.(=) p.(=)
?/? c.1340-25_1340-24insT r.(=) p.(=)
?/? c.1340-13T>C r.(=) p.(=)
?/? c.1358C>T r.(?) p.(Ser453Leu)
?/? c.1410G>A r.(=) p.(=)
?/? c.1414G>C r.(?) p.(Glu472Gln)
?/? c.1434C>A r.(?) p.(Asn478Lys)
?/? c.1436-12T>A r.(=) p.(=)
?/? c.1441G>A r.(?) p.(Val481Ile)
?/? c.1483A>G r.(?) p.(Lys495Glu)
?/? c.1519G>A r.(?) p.(Val507Met)
?/? c.1549A>G r.(?) p.(Ile517Val)
?/? c.1554G>A r.(=) p.(=)
?/? c.1568C>T r.(?) p.(Thr523Met)
?/? c.1572A>C r.(=) p.(=)
?/? c.1573C>T r.(=) p.(=)
?/? c.1603A>G r.(?) p.(Thr535Ala)
?/? c.1632C>T r.(=) p.(=)
?/? c.1633G>A r.(?) p.(Asp545Asn)
?/? c.1645+17A>G r.(=) p.(=)
?/? c.1645+27C>T r.(=) p.(=)
?/? c.1645+40C>T r.(=) p.(=)
?/? c.1645+43G>A r.(=) p.(=)
?/? c.1646-30G>A r.(=) p.(=)
?/? c.1646-14_1646-10del r.(=) p.(=)
?/? c.1676G>A r.(?) p.(Arg559His)
?/? c.1722T>A r.(?) p.(Ser574Arg)
?/? c.1726-43A>C r.(=) p.(=)
?/? c.1726-27G>A r.(=) p.(=)
?/? c.1726-7T>A r.(=) p.(=)
?/? c.1865G>C r.(?) p.(Gly622Ala)
?/? c.1890G>T r.(?) p.(Lys630Asn)
?/? c.1906+15T>C r.(=) p.(=)
?/? c.1906+39C>A r.(=) p.(=)
?/? c.1906+47C>G r.(=) p.(=)
?/? c.1907-33A>G r.(=) p.(=)
?/? c.1950+13C>T r.(=) p.(=)
?/? c.1950+29T>C r.(=) p.(=)
?/? c.1950+34T>G r.(=) p.(=)
?/? c.1950+37G>T r.(=) p.(=)
?/? c.1951-48T>A r.(=) p.(=)
?/? c.1951-27A>G r.(=) p.(=)
?/? c.1951-8T>A r.(=) p.(=)
?/? c.1957A>G r.(?) p.(Lys653Glu)
?/? c.1968C>G r.(=) p.(=)
?/? c.1986-40C>T r.(=) p.(=)
?/? c.1986-36C>T r.(=) p.(=)
?/? c.1986-35G>A r.(=) p.(=)
?/? c.1986-33C>A r.(=) p.(=)
?/? c.2000A>G r.(?) p.(Glu667Gly)
?/? c.2023G>A r.(?) p.(Ala675Thr)
?/? c.2038_2039insCTGA r.(?) p.(Met680Thrfs*18)
?/? c.2090A>G r.(?) p.(Asn697Ser)
?/? c.2132A>C r.(?) p.(Glu711Ala)
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