Transcript #00025503 (NM_001130955.1, ARHGEF18 gene)

Transcript name transcript variant 2
Gene name ARHGEF18 (Rho/Rac guanine nucleotide exchange factor (GEF) 18)
Chromosome 19
Transcript - NCBI ID NM_001130955.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001124427.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2020-04-18 10:18:00 +02:00 (CEST)
Date last edited N/A


Variants

92 entries on 1 page. Showing entries 1 - 92.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-67111C>T r.(?) p.(=)
?/. - c.-67099A>C r.(?) p.(=)
-?/. - c.-66873G>A r.(?) p.(=)
?/. - c.-63259G>A r.(?) p.(=)
?/. - c.-57066T>C r.(?) p.(=)
?/. - c.-57066T>C r.(?) p.(=)
-?/. - c.45T>A r.(?) p.(Ala15=)
-?/. - c.114C>A r.(?) p.(Gly38=)
-?/. - c.131C>G r.(?) p.(Ala44Gly)
+?/. - c.343G>A r.(?) p.(Gly115Arg)
?/. - c.343G>A r.(?) p.(Gly115Arg)
?/. - c.359C>T r.(?) p.(Pro120Leu)
?/. - c.442G>T r.(?) p.(Asp148Tyr)
-?/. - c.506C>A r.(?) p.(Pro169Gln)
?/. - c.541G>A r.(?) p.(Gly181Arg)
-?/. - c.541G>A r.(?) p.(Gly181Arg)
-?/. - c.636C>T r.(?) p.(Thr212=)
-?/. - c.655+14C>T r.(=) p.(=)
-?/. - c.658C>T r.(?) p.(Pro220Ser)
-?/. - c.658C>T r.(?) p.(Pro220Ser)
-?/. - c.714T>C r.(?) p.(Ala238=)
-?/. - c.794A>T r.(?) p.(Tyr265Phe)
-?/. - c.796+20G>A r.(=) p.(=)
+/. - c.808A>G r.(?) p.(Thr270Ala)
+?/. - c.808A>G r.(?) p.(Thr270Ala)
?/. - c.812C>T r.(?) p.(Thr271Met)
-/. - c.822C>T r.(?) p.(His274=)
?/. - c.827G>A r.(?) p.(Arg276Gln)
?/. - c.1039G>A r.(?) p.(Val347Ile)
?/. - c.1039G>A r.(?) p.(Val347Ile)
?/. - c.1135C>G r.(?) p.(Leu379Val)
-/. - c.1173+21dup r.(=) p.(=)
-/. - c.1174-11C>G r.(=) p.(=)
?/. - c.1185C>G r.(?) p.(Asn395Lys)
+?/. - c.1210G>A r.(?) p.(Val404Met)
?/. - c.1276A>C r.(?) p.(Ile426Leu)
+?/. - c.1286C>T r.(?) p.(Thr429Met)
?/. - c.1408G>A r.(?) p.(Ala470Thr)
?/. - c.1463G>A r.(?) p.(Arg488His)
?/. - c.1523C>T r.(?) p.(Thr508Ile)
?/. - c.1523C>T r.(?) p.(Thr508Ile)
-?/. - c.1602C>T r.(?) p.(Tyr534=)
+/. - c.1617+5G>A r.[1541_1617del,=] p.[Asp540Gly*37,=]
?/. - c.1725G>A r.(?) p.(Met575Ile)
?/. - c.1888+4A>T r.spl? p.?
?/. - c.1888+4A>T r.spl p.?
-?/. - c.1888+7G>A r.(=) p.(=)
+/. - c.1889-1G>A r.spl? p.?
-?/. - c.1956G>A r.(?) p.(Glu652=)
-/. - c.1956G>A r.(?) p.(Glu652=)
-?/. - c.1977C>G r.(?) p.(Leu659=)
+/. - c.1996C>T r.(?) p.(Arg666*)
+?/. - c.1996C>T r.(?) p.(Arg666*)
-?/. - c.2046A>G r.(?) p.(Leu682=)
-?/. - c.2046A>G r.(?) p.(Leu682=)
-?/. - c.2058G>A r.(?) p.(=)
-?/. - c.2067C>T r.(?) p.(Ser689=)
-/. - c.2112C>T r.(?) p.(Ser704=)
-?/. - c.2118C>T r.(?) p.(Asn706=)
-?/. - c.2126C>T r.(?) p.(Ala709Val)
-/. - c.2145C>T r.(?) p.(Ser715=)
-/. - c.2280C>T r.(?) p.(Ser760=)
+?/. - c.2341-1G>T r.spl? p.?
?/. - c.2393C>T r.(?) p.(Ser798Leu)
-?/. - c.2393C>T r.(?) p.(Ser798Leu)
-?/. - c.2554C>A r.(?) p.(Gln852Lys)
-?/. - c.2604G>C r.(?) p.(Leu868=)
-/. - c.2604G>C r.(?) p.(Leu868=)
+/. - c.2632G>T r.(?) p.(Glu878*)
+?/. - c.2632G>T r.(?) p.(Glu878*)
+/. - c.2738_2761del r.(?) p.(Arg913_Glu920del)
+?/. - c.2738_2761del r.(?) p.(Arg913_Glu920del)
-?/. - c.2757C>G r.(?) p.(Ala919=)
-?/. - c.2763G>T r.(?) p.(Leu921=)
?/. - c.2790C>G r.(?) p.(His930Gln)
-?/. - c.2992G>A r.(?) p.(Gly998Ser)
?/. - c.2992G>A r.(?) p.(Gly998Ser)
?/. - c.3017G>A r.(?) p.(Arg1006His)
?/. - c.3035G>A r.(?) p.(Arg1012Gln)
-?/. - c.3097G>A r.(?) p.(Ala1033Thr)
-?/. - c.3097G>A r.(?) p.(Ala1033Thr)
-?/. - c.3187G>A r.(?) p.(Gly1063Ser)
-?/. - c.3219C>T r.(?) p.(Ser1073=)
-?/. - c.3219C>T r.(?) p.(Ser1073=)
?/. - c.3284C>A r.(?) p.(Thr1095Asn)
?/. - c.3296G>A r.(?) p.(Arg1099His)
?/. - c.3298C>T r.(?) p.(Arg1100Cys)
-?/. - c.3417C>T r.(?) p.(Ala1139=)
-?/. - c.3418G>A r.(?) p.(Gly1140Arg)
?/. - c.3418G>A r.(?) p.(Gly1140Arg)
?/. - c.3418G>A r.(?) p.(Gly1140Arg)
-?/. - c.3444C>G r.(?) p.(Pro1148=)
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