Transcript #00008841 (NM_145290.3, GPR125 gene)

Transcript name G protein-coupled receptor 125
Gene name GPR125 (G protein-coupled receptor 125)
Chromosome 4
Transcript - NCBI ID NM_145290.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_660333.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

87 entries on 1 page. Showing entries 1 - 87.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.98_106del r.(?) p.(Gly33_Gly35del)
-?/. - c.102C>A r.(?) p.(Gly34=)
?/. - c.104_106del r.(?) p.(Gly35del)
?/. - c.169G>A r.(?) p.(Gly57Ser)
?/. - c.470G>A r.(?) p.(Arg157Gln)
-/. - c.478C>A r.(?) p.(Leu160Ile)
+?/. - c.560A>C r.(?) p.(Glu187Ala)
?/. - c.599G>A r.(?) p.(Arg200His)
?/. - c.599G>A r.(?) p.(Arg200His)
-/. - c.681C>T r.(?) p.(Gly227=)
-?/. - c.726G>A r.(?) p.(Pro242=)
?/. - c.808G>C r.(?) p.(Asp270His)
?/. - c.819G>T r.(?) p.(Met273Ile)
?/. - c.859G>A r.(?) p.(Asp287Asn)
-/. - c.859G>A r.(?) p.(Asp287Asn)
+?/. - c.859G>A r.(?) p.(Asp287Asn)
-?/. - c.866C>T r.(?) p.(Ser289Leu)
-?/. - c.920+13T>A r.(=) p.(=)
-/. - c.920+20_920+21del r.(=) p.(=)
?/. - c.950G>A r.(?) p.(Gly317Glu)
?/. - c.989G>A r.(?) p.(Arg330His)
?/. - c.989G>A r.(?) p.(Arg330His)
-?/. - c.1049C>T r.(?) p.(Pro350Leu)
?/. - c.1049C>T r.(?) p.(Pro350Leu)
-/. - c.1086-17T>G r.(=) p.(=)
-?/. - c.1090C>T r.(?) p.(Pro364Ser)
-?/. - c.1325_1326insCCACAGCTCG r.(?) p.(Gln443HisfsTer17)
-/. - c.1416A>G r.(?) p.(Arg472=)
-?/. - c.1443+7_1443+9del r.(=) p.(=)
-?/. - c.1582G>A r.(?) p.(Gly528Ser)
-/. - c.1582G>A r.(?) p.(Gly528Ser)
?/. - c.1582G>A r.(?) p.(Gly528Ser)
-?/. - c.1590T>C r.(?) p.(Ala530=)
-?/. - c.1638C>T r.(?) p.(Val546=)
+?/. - c.1659G>A r.[(=,1755_1809del)] p.?
?/. - c.1703G>A r.(?) p.(Arg568His)
?/. - c.1706C>T r.(?) p.(Thr569Ile)
?/. - c.2000C>T r.(?) p.(Thr667Ile)
?/. - c.2264C>T r.(?) p.(Ala755Val)
?/. - c.2264C>T r.(?) p.(Ala755Val)
-?/. - c.2302A>G r.(?) p.(Ile768Val)
+?/. - c.2392C>T r.(?) p.(Leu798Phe)
-?/. - c.2392C>T r.(?) p.(Leu798Phe)
+?/. - c.2431G>T r.(?) p.(Val811Phe)
+?/. - c.2431G>T r.(?) p.(Val811Phe)
+/. 17 c.2504C>G r.(?) p.(Ser835Cys)
+?/. - c.2504C>G r.(?) p.(Ser835Cys)
-/. - c.2553C>T r.(?) p.(Tyr851=)
?/. - c.2556A>C r.(?) p.(Lys852Asn)
?/. - c.2556A>C r.(?) p.(Lys852Asn)
?/. - c.2601dup r.(?) p.(Pro868ThrfsTer31)
-?/. - c.2620A>G r.(?) p.(Met874Val)
-/. - c.2667C>T r.(?) p.(Cys889=)
+?/. - c.2689A>G r.(?) p.(Ile897Val)
?/. - c.2720C>A r.(?) p.(Pro907His)
?/. 19 c.2801A>G r.(?) p.(Tyr934Cys)
+?/. - c.2801A>G r.(?) p.(Tyr934Cys)
?/. - c.2801A>G r.(?) p.(Tyr934Cys)
+?/. - c.2843G>A r.(?) p.(Arg948His)
-?/. - c.2901T>C r.(?) p.(=)
-?/. - c.3015A>G r.(?) p.(Leu1005=)
?/. - c.3044T>C r.(?) p.(Leu1015Ser)
-/. - c.3090T>A r.(?) p.(Val1030=)
-?/. - c.3120G>A r.(?) p.(Ala1040=)
?/. - c.3127G>A r.(?) p.(Val1043Met)
?/. - c.3127G>A r.(?) p.(Val1043Met)
?/. - c.3245C>T r.(?) p.(Thr1082Met)
?/. - c.3245C>T r.(?) p.(Thr1082Met)
?/. 19 c.3281C>T r.(?) p.(Ala1094Val)
?/. - c.3281C>T r.(?) p.(Ala1094Val)
?/. 19 c.3281C>T r.(?) p.(Ala1094Val)
-/. - c.3468G>A r.(?) p.(Ala1156=)
-?/. - c.3480T>C r.(?) p.(Val1160=)
?/. - c.3497T>G r.(?) p.(Val1166Gly)
?/. - c.3497T>G r.(?) p.(Val1166Gly)
-/. - c.3555A>T r.(?) p.(Thr1185=)
-?/. - c.3587C>G r.(?) p.(Thr1196Arg)
?/. - c.3587C>G r.(?) p.(Thr1196Arg)
?/. 19 c.3592G>A r.(?) p.(Val1198Met)
?/. - c.3592G>A r.(?) p.(Val1198Met)
?/. - c.3662G>A r.(?) p.(Arg1221Gln)
+?/. - c.3668C>T r.(?) p.(Ala1223Val)
-?/. - c.3826A>C r.(?) p.(Asn1276His)
?/. - c.3893A>C r.(?) p.(Glu1298Ala)
?/. - c.3907G>A r.(?) p.(Gly1303Ser)
?/. - c.3907G>T r.(?) p.(Gly1303Cys)
-/. - c.*17A>G r.(=) p.(=)
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