Transcript #00000649 (NM_013427.2, ARHGAP6 gene)

Transcript name transcript variant 1
Gene name ARHGAP6 (Rho GTPase activating protein 6)
Chromosome X
Transcript - NCBI ID NM_013427.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_038286.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2012-09-13 12:43:49 +02:00 (CEST)
Date last edited N/A


Variants

56 entries on 1 page. Showing entries 1 - 56.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.-127T>C r.(?) p.(=)
?/. - c.-127T>C r.(?) p.(=)
?/. _1_13_ c.(-1_*1)::[NM_001101802.1:(-1_*1) r.? p.?
?/. - c.329A>G r.(?) p.(Gln110Arg)
-?/. - c.386G>A r.(?) p.(Gly129Asp)
-?/. - c.479G>T r.(?) p.(Gly160Val)
-?/. - c.589-45895A>G r.(=) p.(=)
?/. - c.589-44259T>G r.(=) p.(=)
-?/. - c.589-44235G>T r.(=) p.(=)
?/. - c.589-44190T>C r.(=) p.(=)
?/. - c.589-44190T>C r.(=) p.(=)
-?/. - c.589-44170C>T r.(=) p.(=)
-/. - c.589-44132C>A r.(=) p.(=)
?/. - c.589-44126del r.(=) p.(=)
?/. - c.589-44111G>C r.(=) p.(=)
-?/. - c.589-44062G>A r.(=) p.(=)
./. - c.589-43915G>A r.(=) p.(=)
?/. - c.589-43895G>A r.(=) p.(=)
?/. - c.589-43881T>C r.(=) p.(=)
?/. - c.589-43867C>T r.(=) p.(=)
?/. - c.589-40200A>G r.(=) p.(=)
?/. - c.589-40200A>G r.(=) p.(=)
?/. - c.589-10998C>T r.(=) p.(=)
?/. - c.589-10998C>T r.(=) p.(=)
?/. - c.589-8del r.(=) p.(=)
?/. - c.589-8del r.(=) p.(=)
?/. - c.638C>T r.(?) p.(Ser213Leu)
?/. - c.748+26748del r.(=) p.(=)
-?/. - c.897C>T r.(?) p.(Asp299=)
?/. - c.910G>A r.(?) p.(Glu304Lys)
?/. - c.941C>T r.(?) p.(Ser314Phe)
?/. - c.949C>A r.(?) p.(Pro317Thr)
?/. - c.1034C>T r.(?) p.(Thr345Met)
-?/. - c.1035G>A r.(?) p.(Thr345=)
?/. - c.1329+112dup r.(=) p.(=)
?/. - c.1330-178_1330-177del r.(=) p.(=)
-?/. - c.1349G>A r.(?) p.(Arg450His)
?/. - c.1355T>C r.(?) p.(Ile452Thr)
?/. - c.1435C>T r.(?) p.(Pro479Ser)
-?/. - c.1455G>A r.(?) p.(Leu485=)
-?/. - c.1600G>A r.(?) p.(Asp534Asn)
?/. - c.1630-88del r.(=) p.(=)
?/. - c.1739G>A r.(?) p.(Arg580Gln)
?/. - c.1739G>A r.(?) p.(Arg580Gln)
?/. - c.2036G>A r.(?) p.(Arg679His)
?/. - c.2177A>T r.(?) p.(Asp726Val)
-?/. - c.2191C>A r.(?) p.(Pro731Thr)
-?/. - c.2289C>A r.(=) p.(=)
?/. - c.2373C>G r.(?) p.(Asp791Glu)
?/. - c.2495G>A r.(?) p.(Arg832Gln)
-?/. - c.2495G>A r.(?) p.(Arg832Gln)
-?/. - c.2502G>A r.(?) p.(Thr834=)
-?/. - c.2698C>T r.(?) p.(Pro900Ser)
?/. - c.2750G>A r.(?) p.(Arg917Gln)
-?/. - c.2754G>T r.(?) p.(Glu918Asp)
-?/. - c.2857G>C r.(?) p.(Glu953Gln)
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