Transcript #00002795 (NM_020754.2, ARHGAP31 gene)

Transcript name Rho GTPase activating protein 31
Gene name ARHGAP31 (Rho GTPase activating protein 31)
Chromosome 3
Transcript - NCBI ID NM_020754.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_065805.2
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

78 entries on 1 page. Showing entries 1 - 78.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.100+9C>T r.(=) p.(=)
?/. - c.118A>G r.(?) p.(Ser40Gly)
?/. - c.185C>T r.(?) p.(Ser62Leu)
?/. - c.185C>T r.(?) p.(Ser62Leu)
-?/. - c.203+6C>T r.(=) p.(=)
-?/. - c.203+9A>C r.(=) p.(=)
?/. - c.230C>T r.(?) p.(Pro77Leu)
-?/. - c.349-7T>G r.(=) p.(=)
-?/. - c.349-7T>G r.(=) p.(=)
-?/. - c.349-7T>G r.(=) p.(=)
-?/. - c.499G>A r.(?) p.(Ala167Thr)
-?/. - c.503G>A r.(?) p.(Arg168Gln)
?/. - c.539+2T>C r.spl? p.?
?/. - c.614T>C r.(?) p.(Ile205Thr)
?/. - c.662C>T r.(?) p.(Pro221Leu)
-?/. - c.662C>T r.(?) p.(Pro221Leu)
-?/. - c.662C>T r.(?) p.(Pro221Leu)
?/. - c.700A>G r.(?) p.(Lys234Glu)
-?/. - c.820C>T r.(?) p.(Pro274Ser)
-/. - c.820C>T r.(?) p.(Pro274Ser)
-?/. - c.936T>C r.(?) p.(=)
-?/. - c.953A>G r.(?) p.(Lys318Arg)
-?/. - c.1004C>T r.(?) p.(Ser335Leu)
?/. - c.1004C>T r.(?) p.(Ser335Leu)
-/. - c.1065A>G r.(?) p.(Val355=)
?/. - c.1217G>T r.(?) p.(Gly406Val)
?/. - c.1220C>A r.(?) p.(Ala407Asp)
-?/. - c.1267G>C r.(?) p.(Ala423Pro)
-?/. - c.1280C>G r.(?) p.(Pro427Arg)
?/. - c.1283C>G r.(?) p.(Pro428Arg)
?/. - c.1320T>A r.(?) p.(Asp440Glu)
-?/. - c.1402A>G r.(?) p.(Ser468Gly)
-?/. - c.1432C>T r.(?) p.(Arg478Cys)
?/. - c.1519A>G r.(?) p.(Thr507Ala)
-?/. - c.1537C>T r.(?) p.(Pro513Ser)
-?/. - c.1539G>A r.(?) p.(Pro513=)
-?/. - c.1700C>T r.(?) p.(Pro567Leu)
-/. - c.1701G>A r.(?) p.(Pro567=)
+?/. - c.1801G>T r.(?) p.(Glu601Ter)
-/. - c.1926+5A>G r.spl? p.?
-/. - c.1926+11T>C r.(=) p.(=)
?/. - c.2042C>G r.(?) p.(Pro681Arg)
+/. 12 c.2047C>T r.(?) p.(Gln683*)
-?/. - c.2140C>T r.(?) p.(Pro714Ser)
-?/. - c.2180C>T r.(?) p.(Thr727Ile)
-?/. 12 c.2180C>T r.(?) p.(Thr727Ile)
+?/. 12 c.2193del r.(?) p.(Thr732Glnfs*26)
-?/. - c.2312T>C r.(?) p.(Val771Ala)
-?/. - c.2323G>A r.(?) p.(Gly775Ser)
-?/. - c.2344C>A r.(?) p.(Pro782Thr)
-/. - c.2407G>A r.(?) p.(Gly803Ser)
-?/. - c.2411C>T r.(?) p.(Pro804Leu)
-?/. - c.2463G>C r.(?) p.(Gln821His)
-?/. - c.2777C>T r.(?) p.(Ala926Val)
?/. - c.2792T>A r.(?) p.(Val931Glu)
-?/. - c.2814G>T r.(?) p.(Gln938His)
-?/. - c.2839C>T r.(?) p.(Pro947Ser)
+?/. - c.2890C>T r.(?) p.(Gln964Ter)
-?/. - c.2972C>A r.(?) p.(Ala991Glu)
-?/. - c.3104C>T r.(?) p.(Thr1035Ile)
./. - c.3127G>A r.(?) p.(Gly1043Arg)
-?/. - c.3148_3156del r.(?) p.(Leu1050_His1052del)
?/. - c.3148_3156del r.(?) p.(Leu1050_His1052del)
?/. - c.3229G>A r.(?) p.(Asp1077Asn)
-?/. - c.3255C>T r.(?) p.(Pro1085=)
-?/. - c.3256G>A r.(?) p.(Ala1086Thr)
+/. 12 c.3260del r.(?) p.(Lys1087Serfs*4)
-?/. - c.3444T>A r.(?) p.(Ser1148=)
?/. - c.3527G>A r.(?) p.(Arg1176His)
?/. - c.3596C>T r.(?) p.(Ala1199Val)
?/. - c.3679C>G r.(?) p.(Gln1227Glu)
-?/. - c.3683C>T r.(?) p.(Pro1228Leu)
-?/. - c.3749A>T r.(?) p.(Asp1250Val)
-?/. - c.3802G>A r.(?) p.(Gly1268Arg)
-?/. - c.3802G>A r.(?) p.(Gly1268Arg)
-?/. - c.3803G>A r.(?) p.(Gly1268Glu)
-?/. - c.3882G>A r.(?) p.(Ser1294=)
-?/. - c.4066A>G r.(?) p.(Ile1356Val)
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