Transcript #00006778

Transcript name transcript variant 1
Gene name GLRA4 (glycine receptor, alpha 4)
Chromosome X
Transcript - NCBI ID NM_001024452.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001019623.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

76 entries on 1 page. Showing entries 1 - 76.
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Affects function     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/? c.72-36T>C r.(=) p.(=)
?/? c.72-16_72-15insT r.(=) p.(=)
?/? c.156G>C r.(?) p.(Met52Ile)
?/? c.160C>T r.(?) p.(Arg54*)
?/? c.202+7A>G r.(=) p.(=)
?/? c.202+28C>T r.(=) p.(=)
?/? c.203-27C>T r.(=) p.(=)
?/? c.203-4T>C r.spl? p.?
?/? c.203G>A r.(?) p.(Gly68Asp)
?/? c.253A>G r.(?) p.(Ile85Val)
?/? c.270+5G>C r.spl? p.?
?/? c.270+27C>T r.(=) p.(=)
?/? c.271-48C>G r.(=) p.(=)
?/? c.271-9C>A r.(=) p.(=)
?/? c.278G>A r.(?) p.(Arg93Gln)
?/? c.313C>T r.(?) p.(Pro105Ser)
?/? c.316C>T r.(?) p.(Arg106Cys)
?/? c.337C>G r.(?) p.(Pro113Ala)
?/? c.363C>G r.(=) p.(=)
?/? c.405T>G r.(=) p.(=)
?/? c.433G>A r.(?) p.(Val145Met)
?/? c.458G>A r.(?) p.(Arg153His)
?/? c.494+7C>T r.(=) p.(=)
?/? c.494+8G>A r.(=) p.(=)
?/? c.494+32G>A r.(=) p.(=)
?/? c.494+41A>C r.(=) p.(=)
?/? c.495-57del r.(=) p.(=)
?/? c.495-41C>T r.(=) p.(=)
?/? c.531G>T r.(?) p.(Lys177Asn)
?/? c.555C>G r.(=) p.(=)
?/? c.577+3A>G r.spl? p.?
?/? c.577+34A>G r.(=) p.(=)
?/? c.577+51C>T r.(=) p.(=)
?/? c.597C>A r.(?) p.(Asp199Glu)
?/? c.601G>A r.(?) p.(Val201Met)
?/? c.673C>T r.(?) p.(Arg225Trp)
?/? c.695G>A r.(?) p.(Cys232Tyr)
?/? c.735C>T r.(=) p.(=)
?/? c.736G>A r.(?) p.(Glu246Lys)
?/? c.757C>T r.(?) p.(Arg253Trp)
?/? c.778A>G r.(?) p.(Ile260Val)
?/? c.799C>T r.(=) p.(=)
?/? c.814C>T r.(=) p.(=)
?/? c.820T>C r.(?) p.(Trp274Arg)
?/? c.845A>T r.(?) p.(Asp282Val)
?/? c.883G>A r.(?) p.(Val295Met)
?/? c.926T>A r.(?) p.(Leu309*)
?/? c.933+17G>C r.(=) p.(=)
?/? c.933+49C>T r.(=) p.(=)
?/? c.934-357C>T r.(=) p.(=)
?/? c.934-331A>G r.(=) p.(=)
?/? c.934-169A>G r.(?) p.(Met116Thr)
?/? c.934-133G>C r.(?) p.(Ala104Gly)
?/? c.934-109T>A r.(?) p.(Glu96Val)
?/? c.934-87C>G r.(?) p.(Ala89Pro)
?/? c.934-59C>A r.(?) p.(Glu79Asp)
?/? c.943G>A r.(?) p.(Arg57Cys)
?/? c.954C>A r.(?) p.(Arg53Leu)
?/? c.955G>A r.(?) p.(Arg53*)
?/? c.970G>T r.(?) p.(Gln48Lys)
?/? c.1031G>A r.(?) p.(Arg344His)
?/? c.1038T>C r.(=) p.(=)
?/? c.1049T>C r.(?) p.(Ile350Thr)
?/? c.1051C>T r.(?) p.(Arg351*)
?/? c.1077A>G r.(=) p.(=)
?/? c.1083+29C>A r.(=) p.(=)
?/? c.1083+1141T>C r.(=) p.(=)
?/? c.1083+1158G>A r.(=) p.(=)
?/? c.1083+1197T>C r.(?) p.(Asn22Ser)
?/? c.1091A>G r.(?) p.(Asp364Gly)
?/? c.1097T>C r.(?) p.(Ile366Thr)
?/? c.1158T>C r.(=) p.(=)
?/? c.1183A>G r.(?) p.(Ile395Val)
?/? c.1189A>T r.(?) p.(Ser397Cys)
?/? c.1233G>T r.(=) p.(=)
?/? c.1246G>A r.(?) p.(Val416Met)
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