Transcript #00010269

Transcript name major facilitator superfamily domain containing 9
Gene name MFSD9 (major facilitator superfamily domain containing 9)
Chromosome 2
Transcript - NCBI ID NM_032718.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_116107.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-32G>C r.(=) p.(=)
?/? c.-30T>A r.(=) p.(=)
?/? c.-16C>A r.(=) p.(=)
?/? c.-15C>T r.(=) p.(=)
?/? c.14G>A r.(?) p.(Gly5Asp)
?/? c.18C>A r.(?) p.(His6Gln)
?/? c.25A>C r.(?) p.(Met9Leu)
?/? c.76C>T r.(?) p.(Gln26*)
?/? c.89C>T r.(?) p.(Thr30Ile)
?/? c.117del r.(?) p.(Val40Serfs*28)
?/? c.127C>T r.(?) p.(Arg43Cys)
?/? c.160T>C r.(?) p.(Phe54Leu)
?/? c.165+8C>G r.(=) p.(=)
?/? c.165+17G>C r.(=) p.(=)
?/? c.165+35G>A r.(=) p.(=)
?/? c.213C>A r.(=) p.(=)
?/? c.253+57A>G r.(=) p.(=)
?/? c.254-20T>C r.(=) p.(=)
?/? c.260C>G r.(?) p.(Ser87Cys)
?/? c.284C>G r.(?) p.(Ser95Cys)
?/? c.298-48A>G r.(=) p.(=)
?/? c.298-45C>T r.(=) p.(=)
?/? c.298-43T>A r.(=) p.(=)
?/? c.298-38G>A r.(=) p.(=)
?/? c.306G>A r.(?) p.(Trp102*)
?/? c.341C>A r.(?) p.(Ala114Glu)
?/? c.375T>G r.(=) p.(=)
?/? c.385G>T r.(?) p.(Ala129Ser)
?/? c.392A>G r.(?) p.(Asn131Ser)
?/? c.408C>T r.(=) p.(=)
?/? c.416G>C r.(?) p.(Arg139Thr)
?/? c.427+33C>T r.(=) p.(=)
?/? c.427+34G>A r.(=) p.(=)
?/? c.428-26A>C r.(=) p.(=)
?/? c.443C>G r.(?) p.(Thr148Ser)
?/? c.445C>G r.(?) p.(Leu149Val)
?/? c.451A>G r.(?) p.(Ile151Val)
?/? c.469T>C r.(?) p.(Ser157Pro)
?/? c.470C>T r.(?) p.(Ser157Phe)
?/? c.473A>G r.(?) p.(Asp158Gly)
?/? c.493C>T r.(?) p.(Arg165Trp)
?/? c.502G>A r.(?) p.(Val168Ile)
?/? c.504A>G r.(=) p.(=)
?/? c.508G>A r.(?) p.(Gly170Arg)
?/? c.513C>T r.(=) p.(=)
?/? c.529G>A r.(?) p.(Gly177Ser)
?/? c.532G>A r.(?) p.(Val178Met)
?/? c.544T>C r.(=) p.(=)
?/? c.563G>T r.(?) p.(Gly188Val)
?/? c.573T>C r.(=) p.(=)
?/? c.576A>G r.(=) p.(=)
?/? c.631A>G r.(?) p.(Asn211Asp)
?/? c.632A>G r.(?) p.(Asn211Ser)
?/? c.637+1G>A r.spl? p.?
?/? c.637+51T>C r.(=) p.(=)
?/? c.638-21G>A r.(=) p.(=)
?/? c.658T>C r.(?) p.(Trp220Arg)
?/? c.704G>A r.(?) p.(Arg235Gln)
?/? c.764G>A r.(?) p.(Arg255His)
?/? c.777C>T r.(=) p.(=)
?/? c.792C>G r.(=) p.(=)
?/? c.801G>A r.(?) p.(Trp267*)
?/? c.842T>C r.(?) p.(Leu281Pro)
?/? c.850G>A r.(?) p.(Glu284Lys)
?/? c.863T>C r.(?) p.(Ile288Thr)
?/? c.910A>G r.(?) p.(Ser304Gly)
?/? c.916T>C r.(?) p.(Phe306Leu)
?/? c.938G>A r.(?) p.(Arg313His)
?/? c.950G>A r.(?) p.(Arg317Gln)
?/? c.964G>A r.(?) p.(Gly322Ser)
?/? c.1000G>A r.(?) p.(Val334Met)
?/? c.1006G>A r.(?) p.(Gly336Ser)
?/? c.1031G>A r.(?) p.(Arg344Gln)
?/? c.1032G>T r.(=) p.(=)
?/? c.1050G>A r.(=) p.(=)
?/? c.1051C>A r.(?) p.(Gln351Lys)
?/? c.1084T>G r.(?) p.(Cys362Gly)
?/? c.1089A>G r.(=) p.(=)
?/? c.1093C>T r.(=) p.(=)
?/? c.1126G>A r.(?) p.(Ala376Thr)
?/? c.1147C>G r.(?) p.(Leu383Val)
?/? c.1187C>T r.(?) p.(Thr396Met)
?/? c.1188G>A r.(=) p.(=)
?/? c.1199T>A r.(?) p.(Leu400Gln)
?/? c.1240G>A r.(?) p.(Val414Met)
?/? c.1276G>A r.(?) p.(Ala426Thr)
?/? c.1285C>T r.(?) p.(Leu429Phe)
?/? c.1289C>T r.(?) p.(Ser430Leu)
?/? c.1317C>T r.(=) p.(=)
?/? c.1318G>A r.(?) p.(Gly440Ser)
?/? c.1321C>G r.(?) p.(Pro441Ala)
?/? c.1322C>A r.(?) p.(Pro441His)
?/? c.1326C>A r.(=) p.(=)
?/? c.1330C>T r.(=) p.(=)
?/? c.1335C>T r.(=) p.(=)
?/? c.1350A>G r.(=) p.(=)
?/? c.1361T>C r.(?) p.(Phe454Ser)
?/? c.1381C>T r.(?) p.(Arg461*)
?/? c.1384C>A r.(?) p.(His462Asn)
?/? c.*16A>T r.(=) p.(=)
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