Transcript #00017476 (NM_001243013.1, ABCB9 gene)

Transcript name ATP-binding cassette, sub-family B (MDR/TAP), member 9, transcript variant 6
Gene name ABCB9 (ATP binding cassette subfamily B member 9)
Chromosome 12
Transcript - NCBI ID NM_001243013.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001229942.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2017-08-08 09:45:52 +02:00 (CEST)
Date last edited N/A


Variants

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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. c.-49C>A r.(=) p.(=)
./. c.-49C>T r.(=) p.(=)
./. c.-46G>A r.(=) p.(=)
./. c.-39A>C r.(=) p.(=)
./. c.-29delT r.(=) p.(=)
./. c.-27A>G r.(=) p.(=)
./. c.-21C>T r.(=) p.(=)
./. c.-12C>A r.(=) p.(=)
./. c.-4C>T r.(=) p.(=)
./. c.-1G>T r.(=) p.(=)
./. c.1429delCinsT r.(?) p.(Pro477Ser)
./. c.*34delGinsA r.(=) p.(=)
./. c.239delGinsA r.(?) p.(Arg80Gln)
./. c.2080delGinsA r.(?) p.(Glu694Lys)
./. c.1380+2delTinsC r.spl? p.?
./. c.716+40delGinsC r.(=) p.(=)
./. c.1775delGinsA r.(?) p.(Arg592Gln)
./. c.-28delCinsT r.(=) p.(=)
./. c.1592delGinsA r.(?) p.(Arg531His)
./. c.1555-11delCinsT r.(=) p.(=)
./. c.4C>T r.(?) p.(Arg2Trp)
./. c.5G>A r.(?) p.(Arg2Gln)
./. c.16G>T r.(?) p.(Ala6Ser)
./. c.17C>T r.(?) p.(Ala6Val)
./. c.19G>A r.(?) p.(Val7Met)
./. c.20T>C r.(?) p.(Val7Ala)
./. c.20T>G r.(?) p.(Val7Gly)
./. c.22_27del r.(?) p.(Val8_Val9del)
./. c.23T>C r.(?) p.(Val8Ala)
./. c.24G>A r.(?) p.(Val8=)
./. c.34G>A r.(?) p.(Ala12Thr)
./. c.36C>A r.(?) p.(Ala12=)
./. c.37T>G r.(?) p.(Phe13Val)
./. c.38T>C r.(?) p.(Phe13Ser)
./. c.42G>A r.(?) p.(Met14Ile)
./. c.44G>T r.(?) p.(Ser15Ile)
./. c.45T>C r.(?) p.(Ser15=)
./. c.47T>C r.(?) p.(Val16Ala)
./. c.50A>G r.(?) p.(Asp17Gly)
./. c.57C>T r.(?) p.(Cys19=)
./. c.65C>T r.(?) p.(Thr22Met)
./. c.66G>A r.(?) p.(Thr22=)
./. c.73T>A r.(?) p.(Tyr25Asn)
./. c.74A>C r.(?) p.(Tyr25Ser)
./. c.93C>G r.(?) p.(Asp31Glu)
./. c.94C>T r.(?) p.(Arg32Cys)
./. c.95G>A r.(?) p.(Arg32His)
./. c.96C>T r.(?) p.(Arg32=)
./. c.96C>G r.(?) p.(Arg32=)
./. c.103C>T r.(?) p.(Leu35=)
./. c.110A>T r.(?) p.(Asp37Val)
./. c.115C>G r.(?) p.(Arg39Gly)
./. c.115C>T r.(?) p.(Arg39Cys)
./. c.116G>A r.(?) p.(Arg39His)
./. c.120C>T r.(?) p.(His40=)
./. c.122T>G r.(?) p.(Phe41Cys)
./. c.131T>C r.(?) p.(Phe44Ser)
./. c.137C>T r.(?) p.(Ser46Leu)
./. c.138G>A r.(?) p.(Ser46=)
./. c.144G>A r.(?) p.(Leu48=)
./. c.154G>A r.(?) p.(Ala52Thr)
./. c.154G>C r.(?) p.(Ala52Pro)
./. c.162C>T r.(?) p.(Cys54=)
./. c.163C>T r.(?) p.(Leu55=)
./. c.169C>A r.(?) p.(Arg57Ser)
./. c.169C>T r.(?) p.(Arg57Cys)
./. c.182T>A r.(?) p.(Leu61Gln)
./. c.183G>C r.(?) p.(Leu61=)
./. c.186G>C r.(?) p.(Leu62=)
./. c.191C>T r.(?) p.(Ala64Val)
./. c.194C>T r.(?) p.(Thr65Ile)
./. c.197T>C r.(?) p.(Ile66Thr)
./. c.214A>G r.(?) p.(Ser72Gly)
./. c.216T>G r.(?) p.(Ser72Arg)
./. c.218C>T r.(?) p.(Ala73Val)
./. c.219G>A r.(?) p.(Ala73=)
./. c.219G>T r.(?) p.(Ala73=)
./. c.226C>G r.(?) p.(Pro76Ala)
./. c.227C>T r.(?) p.(Pro76Leu)
./. c.229C>A r.(?) p.(Arg77=)
./. c.229C>T r.(?) p.(Arg77Trp)
./. c.230G>A r.(?) p.(Arg77Gln)
./. c.232C>T r.(?) p.(Arg78Trp)
./. c.233G>A r.(?) p.(Arg78Gln)
./. c.238delC r.(?) p.(Arg80GlyfsTer20)
./. c.238C>T r.(?) p.(Arg80Trp)
./. c.244T>C r.(?) p.(Ser82Pro)
./. c.245C>T r.(?) p.(Ser82Leu)
./. c.246G>A r.(?) p.(Ser82=)
./. c.246G>C r.(?) p.(Ser82=)
./. c.249G>C r.(?) p.(Trp83Cys)
./. c.251T>A r.(?) p.(Leu84Gln)
./. c.260C>T r.(?) p.(Thr87Ile)
./. c.264C>T r.(?) p.(Leu88=)
./. c.265G>A r.(?) p.(Val89Met)
./. c.276C>A r.(?) p.(Phe92Leu)
./. c.276C>T r.(?) p.(Phe92=)
./. c.277G>A r.(?) p.(Val93Met)
./. c.277G>T r.(?) p.(Val93Leu)
./. c.280G>A r.(?) p.(Gly94Ser)
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