Transcript #00013976

Transcript name transcript variant 1
Gene name PCDHGA4 (protocadherin gamma subfamily A, 4)
Chromosome 5
Transcript - NCBI ID NM_018917.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_061740.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

1794 entries on 18 pages. Showing entries 1 - 100.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.6G>T r.(=) p.(=)
?/? c.35G>C r.(?) p.(Arg12Pro)
?/? c.40C>T r.(?) p.(Leu14Phe)
?/? c.44A>G r.(?) p.(Gln15Arg)
?/? c.62G>A r.(?) p.(Gly21Glu)
?/? c.64G>T r.(?) p.(Val22Phe)
?/? c.88C>G r.(?) p.(Gln30Glu)
?/? c.98A>C r.(?) p.(Tyr33Ser)
?/? c.137G>A r.(?) p.(Gly46Asp)
?/? c.178G>C r.(?) p.(Ala60Pro)
?/? c.193C>T r.(?) p.(Arg65Cys)
?/? c.226G>T r.(?) p.(Ala76Ser)
?/? c.252G>T r.(?) p.(Leu84Phe)
?/? c.287G>A r.(?) p.(Cys96Tyr)
?/? c.316C>T r.(=) p.(=)
?/? c.325C>G r.(?) p.(Leu109Val)
?/? c.388C>T r.(?) p.(Pro130Ser)
?/? c.399T>G r.(?) p.(Phe133Leu)
?/? c.440A>C r.(?) p.(Asn147Thr)
?/? c.448G>A r.(?) p.(Ala150Thr)
?/? c.454T>C r.(?) p.(Phe152Leu)
?/? c.569A>C r.(?) p.(Lys190Thr)
?/? c.615G>A r.(=) p.(=)
?/? c.638C>A r.(?) p.(Thr213Lys)
?/? c.649G>T r.(?) p.(Gly217*)
?/? c.670G>T r.(?) p.(Gly224Cys)
?/? c.732G>T r.(?) p.(Gln244His)
?/? c.834G>A r.(=) p.(=)
?/? c.983G>A r.(?) p.(Arg328Gln)
?/? c.1029C>T r.(=) p.(=)
?/? c.1034C>T r.(?) p.(Pro345Leu)
?/? c.1090A>G r.(?) p.(Thr364Ala)
?/? c.1149A>T r.(=) p.(=)
?/? c.1208G>A r.(?) p.(Arg403Gln)
?/? c.1249G>T r.(?) p.(Glu417*)
?/? c.1379A>G r.(?) p.(Tyr460Cys)
?/? c.1385C>G r.(?) p.(Pro462Arg)
?/? c.1420A>G r.(?) p.(Met474Val)
?/? c.1519A>G r.(?) p.(Ile507Val)
?/? c.1585C>A r.(?) p.(Gln529Lys)
?/? c.1601C>G r.(?) p.(Ala534Gly)
?/? c.1630A>G r.(?) p.(Ser544Gly)
?/? c.1667A>G r.(?) p.(Asn556Ser)
?/? c.1707T>G r.(=) p.(=)
?/? c.1710T>A r.(?) p.(Asp570Glu)
?/? c.1712G>C r.(?) p.(Gly571Ala)
?/? c.1727A>G r.(?) p.(Glu576Gly)
?/? c.1743C>T r.(=) p.(=)
?/? c.1744G>T r.(?) p.(Ala582Ser)
?/? c.1752C>T r.(=) p.(=)
?/? c.1768A>G r.(?) p.(Lys590Glu)
?/? c.1787G>A r.(?) p.(Arg596Lys)
?/? c.1795G>T r.(?) p.(Gly599Cys)
?/? c.1814C>A r.(?) p.(Ser605Tyr)
?/? c.1922G>A r.(?) p.(Arg641Lys)
?/? c.1959T>A r.(=) p.(=)
?/? c.2021A>G r.(?) p.(Asp674Gly)
?/? c.2047G>C r.(?) p.(Asp683His)
?/? c.2061G>C r.(=) p.(=)
?/? c.2080G>A r.(?) p.(Val694Met)
?/? c.2089G>C r.(?) p.(Val697Leu)
?/? c.2127G>A r.(=) p.(=)
?/? c.2129T>C r.(?) p.(Val710Ala)
?/? c.2133G>A r.(=) p.(=)
?/? c.2134C>T r.(=) p.(=)
?/? c.2167C>A r.(?) p.(Arg723Ser)
?/? c.2169C>A r.(=) p.(=)
?/? c.2176C>T r.(?) p.(His726Tyr)
?/? c.2190C>T r.(=) p.(=)
?/? c.2208T>C r.(=) p.(=)
?/? c.2213C>A r.(?) p.(Ser738*)
?/? c.2252A>T r.(?) p.(Gln751Leu)
?/? c.2258A>G r.(?) p.(Tyr753Cys)
?/? c.2273C>T r.(?) p.(Ser758Phe)
?/? c.2283G>A r.(=) p.(=)
?/? c.2294A>G r.(?) p.(Lys765Arg)
?/? c.2343C>G r.(?) p.(Ser781Arg)
?/? c.2346G>C r.(=) p.(=)
?/? c.2415T>C r.(=) p.(=)
?/? c.2421+24A>G r.(=) p.(=)
?/? c.2421+34G>A r.(=) p.(=)
?/? c.2421+48G>A r.(=) p.(=)
?/? c.2421+2487T>C r.(=) p.(=)
?/? c.2421+2508C>T r.(=) p.(=)
?/? c.2421+2549G>C r.(?) p.(Arg12Pro)
?/? c.2421+2578T>C r.(=) p.(=)
?/? c.2421+2585T>C r.(?) p.(Leu24Ser)
?/? c.2421+2591C>G r.(?) p.(Pro26Arg)
?/? c.2421+2615G>T r.(?) p.(Arg34Leu)
?/? c.2421+2620T>C r.(?) p.(Ser36Pro)
?/? c.2421+2624T>C r.(?) p.(Ile37Thr)
?/? c.2421+2677G>A r.(?) p.(Gly55Arg)
?/? c.2421+2686G>A r.(?) p.(Val58Ile)
?/? c.2421+2702C>A r.(?) p.(Ala63Asp)
?/? c.2421+2710C>G r.(?) p.(Leu66Val)
?/? c.2421+2748C>T r.(=) p.(=)
?/? c.2421+2749C>A r.(?) p.(Pro79Thr)
?/? c.2421+2759_2421+2779del r.(?) p.(Asp83_Arg89del)
?/? c.2421+2786A>G r.(?) p.(Asp91Gly)
?/? c.2421+2800T>C r.(?) p.(Cys96Arg)
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