Transcript #00020386

Transcript name tyrosinase-related protein 1
Gene name TYRP1 (tyrosinase-related protein 1)
Chromosome 9
Transcript - NCBI ID NM_000550.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_000541.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

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

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.-6A>G r.(=) p.(=)
?/? c.9T>C r.(=) p.(=)
?/? c.20T>C r.(?) p.(Leu7Pro)
?/? c.21C>G r.(=) p.(=)
?/? c.67C>T r.(?) p.(Arg23Trp)
?/? c.70G>A r.(?) p.(Ala24Thr)
?/? c.80C>G r.(?) p.(Pro27Arg)
?/? c.85C>T r.(?) p.(Gln29*)
?/? c.92C>G r.(?) p.(Ala31Gly)
?/? c.98T>C r.(?) p.(Val33Ala)
?/? c.164G>A r.(?) p.(Arg55His)
?/? c.199G>A r.(?) p.(Ala67Thr)
?/? c.208G>A r.(?) p.(Ala70Thr)
?/? c.244G>T r.(?) p.(Asp82Tyr)
?/? c.259C>A r.(=) p.(=)
?/? c.278G>A r.(?) p.(Arg93His)
?/? c.286A>T r.(?) p.(Asn96Tyr)
?/? c.306C>T r.(=) p.(=)
?/? c.340C>T r.(?) p.(Arg114Cys)
?/? c.368A>T r.(?) p.(Asp123Val)
?/? c.374G>A r.(?) p.(Arg125Lys)
?/? c.385+21G>C r.(=) p.(=)
?/? c.385+31C>T r.(=) p.(=)
?/? c.385+42C>T r.(=) p.(=)
?/? c.385+47G>C r.(=) p.(=)
?/? c.386-37G>A r.(=) p.(=)
?/? c.386-20T>A r.(=) p.(=)
?/? c.395A>T r.(?) p.(Asn132Ile)
?/? c.406_407insTAAG r.(?) p.(Glu139*)
?/? c.418G>T r.(?) p.(Glu140*)
?/? c.457C>T r.(?) p.(Arg153Cys)
?/? c.458G>A r.(?) p.(Arg153His)
?/? c.497C>G r.(?) p.(Ser166*)
?/? c.506T>C r.(?) p.(Ile169Thr)
?/? c.520G>T r.(?) p.(Gly174Cys)
?/? c.554A>G r.(?) p.(Tyr185Cys)
?/? c.565G>C r.(?) p.(Val189Leu)
?/? c.620G>T r.(?) p.(Ser207Ile)
?/? c.621C>T r.(=) p.(=)
?/? c.627T>A r.(=) p.(=)
?/? c.631G>C r.(?) p.(Val211Leu)
?/? c.651A>T r.(=) p.(=)
?/? c.665C>T r.(?) p.(Thr222Ile)
?/? c.672C>T r.(=) p.(=)
?/? c.684C>T r.(=) p.(=)
?/? c.689G>A r.(?) p.(Arg230His)
?/? c.708+4T>C r.spl? p.?
?/? c.708+12G>A r.(=) p.(=)
?/? c.708+19A>G r.(=) p.(=)
?/? c.708+24G>T r.(=) p.(=)
?/? c.708+27G>T r.(=) p.(=)
?/? c.708+31C>G r.(=) p.(=)
?/? c.708+39A>G r.(=) p.(=)
?/? c.708+46G>A r.(=) p.(=)
?/? c.729T>C r.(=) p.(=)
?/? c.739C>A r.(?) p.(Pro247Thr)
?/? c.759G>A r.(=) p.(=)
?/? c.768T>C r.(=) p.(=)
?/? c.781T>G r.(?) p.(Cys261Gly)
?/? c.785C>T r.(?) p.(Thr262Met)
?/? c.797T>C r.(?) p.(Met266Thr)
?/? c.832A>G r.(?) p.(Ser278Gly)
?/? c.853C>T r.(?) p.(Gln285*)
?/? c.913+5G>A r.spl? p.?
?/? c.913+9C>T r.(=) p.(=)
?/? c.913+18G>T r.(=) p.(=)
?/? c.913+45A>G r.(=) p.(=)
?/? c.914-4G>T r.spl? p.?
?/? c.925G>C r.(?) p.(Gly309Arg)
?/? c.926G>A r.(?) p.(Gly309Glu)
?/? c.936G>C r.(?) p.(Arg312Ser)
?/? c.946G>C r.(?) p.(Ala316Pro)
?/? c.977G>A r.(?) p.(Arg326His)
?/? c.996T>C r.(=) p.(=)
?/? c.1000G>A r.(?) p.(Ala334Thr)
?/? c.1029C>T r.(=) p.(=)
?/? c.1031C>T r.(?) p.(Thr344Met)
?/? c.1037C>G r.(?) p.(Pro346Arg)
?/? c.1054A>G r.(?) p.(Thr352Ala)
?/? c.1074A>G r.(=) p.(=)
?/? c.1081+18G>A r.(=) p.(=)
?/? c.1081+21T>G r.(=) p.(=)
?/? c.1081+31A>T r.(=) p.(=)
?/? c.1082-9T>C r.(=) p.(=)
?/? c.1082-8G>A r.(=) p.(=)
?/? c.1082G>C r.(?) p.(Gly361Ala)
?/? c.1101del r.(?) p.(Lys368Serfs*17)
?/? c.1117G>A r.(?) p.(Val373Ile)
?/? c.1138G>T r.(?) p.(Ala380Ser)
?/? c.1140T>A r.(=) p.(=)
?/? c.1149C>A r.(?) p.(Phe383Leu)
?/? c.1162G>C r.(?) p.(Gly388Arg)
?/? c.1226C>T r.(?) p.(Ala409Val)
?/? c.1261+1G>A r.spl? p.?
?/? c.1261+16A>G r.(=) p.(=)
?/? c.1261+20C>T r.(=) p.(=)
?/? c.1261+25G>A r.(=) p.(=)
?/? c.1261+41G>A r.(=) p.(=)
?/? c.1263T>C r.(=) p.(=)
?/? c.1278A>G r.(=) p.(=)
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