Transcript #00000633 (NM_001666.4, ARHGAP4 gene)

Transcript name transcript variant 2
Gene name ARHGAP4 (Rho GTPase activating protein 4)
Chromosome X
Transcript - NCBI ID NM_001666.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_001657.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

156 entries on 2 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
./. - c.-418250_*462377dup r.0? p.0?
?/. - c.-4586C>T r.(?) p.(=)
-?/. - c.-4553G>A r.(?) p.(=)
?/. - c.-4553G>A r.(?) p.(=)
-?/. - c.-4000G>A r.(?) p.(=)
-?/. - c.-3915G>C r.(?) p.(=)
?/. - c.16A>T r.(?) p.(Lys6Ter)
-/. - c.68-5C>T r.spl? p.?
?/. - c.127C>T r.(?) p.(Arg43Trp)
?/. - c.157A>G r.(?) p.(Met53Val)
-?/. - c.168C>T r.(?) p.(Arg56=)
?/. - c.193C>T r.(?) p.(Arg65Trp)
?/. - c.236G>T r.(?) p.(Gly79Val)
-?/. - c.236G>T r.(?) p.(Gly79Val)
?/. - c.309G>T r.(?) p.(Trp103Cys)
-/. - c.342C>T r.(?) p.(Ser114=)
?/. - c.379C>T r.(?) p.(Pro127Ser)
-?/. - c.381C>T r.(?) p.(Pro127=)
?/. - c.498+65dup r.(=) p.(=)
?/. - c.498+65dup r.(=) p.(=)
?/. - c.498+65dup r.(=) p.(=)
?/. - c.498+65dup r.(=) p.(=)
?/. - c.498+137dup r.(=) p.(=)
?/. - c.498+137dup r.(=) p.(=)
?/. - c.498+137dup r.(=) p.(=)
?/. - c.498+137dup r.(=) p.(=)
?/. - c.509C>T r.(?) p.(Thr170Met)
-?/. - c.557G>A r.(?) p.(Arg186Gln)
?/. - c.670C>A r.(?) p.(Leu224Met)
?/. - c.682-377C>T r.(=) p.(=)
-?/. - c.682-283G>T r.(=) p.(=)
?/. - c.805A>G r.(?) p.(Met269Val)
-?/. - c.811-3C>T r.spl? p.?
?/. - c.878G>A r.(?) p.(Arg293His)
-/. - c.932C>T r.(?) p.(Ala311Val)
-?/. - c.932C>T r.(?) p.(Ala311Val)
?/. - c.941C>G r.(?) p.(Pro314Arg)
-?/. - c.941C>G r.(?) p.(Pro314Arg)
-?/. - c.981C>T r.(?) p.(Thr327=)
-?/. - c.1047C>T r.(?) p.(Cys349=)
-?/. - c.1167C>T r.(?) p.(Ala389=)
?/. - c.1282C>T r.(?) p.(Arg428Trp)
-?/. - c.1308C>T r.(?) p.(Thr436=)
?/. - c.1439+18dup r.(=) p.(=)
?/. - c.1439+18dup r.(=) p.(=)
?/. - c.1439+18dup r.(=) p.(=)
?/. - c.1439+18dup r.(=) p.(=)
?/. - c.1516G>A r.(?) p.(Gly506Arg)
-?/. - c.1533G>A r.(=) p.(=)
?/. - c.1543-62_1543-60del r.(=) p.(=)
?/. - c.1585C>T r.(?) p.(Arg529Cys)
-/. - c.1680A>G r.(?) p.(Arg560=)
-?/. - c.1692A>G r.(?) p.(Pro564=)
-?/. - c.1734C>T r.(?) p.(Ala578=)
-?/. - c.1783C>G r.(?) p.(Pro595Ala)
?/. - c.1875C>T r.(?) p.(=)
-?/. - c.1980C>T r.(?) p.(Phe660=)
-?/. - c.1993C>T r.(?) p.(Leu665=)
-?/. - c.1997C>T r.(?) p.(Pro666Leu)
-?/. - c.2031G>A r.(?) p.(Gln677=)
-/. - c.2036G>A r.(?) p.(Arg679Gln)
-?/. - c.2113G>A r.(?) p.(Val705Ile)
-?/. - c.2142C>T r.(?) p.(Ser714=)
-?/. - c.2175C>T r.(?) p.(Ser725=)
?/. - c.2240G>A r.(?) p.(Gly747Glu)
-?/. - c.2412C>A r.(?) p.(Ala804=)
-?/. - c.2414+6T>C r.(=) p.(=)
?/. - c.2414+6T>C r.(=) p.(=)
?/. - c.2415-65dup r.(=) p.(=)
?/. - c.2415-65dup r.(=) p.(=)
-?/. - c.2415-4G>A r.spl? p.?
-?/. - c.2415-3C>T r.spl? p.?
?/. - c.2455G>T r.(?) p.(Gly819Trp)
?/. - c.2470A>C r.(?) p.(Ser824Arg)
-?/. - c.2470A>C r.(?) p.(Ser824Arg)
?/. - c.2482C>T r.(?) p.(Leu828Phe)
?/. - c.2496G>C r.(?) p.(Glu832Asp)
?/. - c.2507+29dup r.(=) p.(=)
?/. - c.2507+29dup r.(=) p.(=)
?/. - c.2507+29dup r.(=) p.(=)
?/. - c.2507+77dup r.(=) p.(=)
?/. - c.2507+77dup r.(=) p.(=)
?/. - c.2507+77dup r.(=) p.(=)
?/. - c.2507+77dup r.(=) p.(=)
-?/. - c.2550A>G r.(?) p.(Gly850=)
-?/. - c.2560C>T r.(?) p.(Arg854Cys)
?/. - c.2593G>A r.(?) p.(Val865Met)
?/. - c.2611G>A r.(?) p.(Val871Met)
-?/. - c.2741G>T r.(?) p.(Arg914Leu)
-?/. - c.2768G>A r.(?) p.(Arg923Gln)
-?/. - c.2822C>T r.(?) p.(Thr941Met)
?/. - c.*673C>T r.(=) p.(=)
-?/. - c.*1005G>A r.(=) p.(=)
-?/. - c.*1046G>A r.(=) p.(=)
-?/. - c.*1062C>T r.(=) p.(=)
-/. - c.*1062C>T r.(=) p.(=)
-?/. - c.*1062C>T r.(=) p.(=)
-?/. - c.*1080C>T r.(=) p.(=)
-?/. - c.*1081G>A r.(=) p.(=)
-?/. - c.*1100C>T r.(=) p.(=)
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