Transcript #00024376

Transcript name transcript variant 1
Gene name ARMCX4 (armadillo repeat containing, X-linked 4)
Chromosome X
Transcript - NCBI ID NM_001256155.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243084.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

37 entries on 1 page. Showing entries 1 - 37.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
?/. - c.? - r.(=) p.(=)
?/. - c.? - r.(=) p.(=)
?/. - c.? - r.(=) p.(=)
-?/. - c.269A>T likely benign r.(?) p.(Lys90Met)
-?/. - c.979A>G likely benign r.(?) p.(Lys327Glu)
-?/. - c.1504G>A likely benign r.(?) p.(Glu502Lys)
-?/. - c.1504G>A likely benign r.(?) p.(Glu502Lys)
-?/. - c.1586G>A likely benign r.(?) p.(Arg529Lys)
?/. - c.1939A>G VUS r.(?) p.(Lys647Glu)
-?/. - c.2254G>A likely benign r.(?) p.(Ala752Thr)
-?/. - c.2436G>T likely benign r.(?) p.(Trp812Cys)
-?/. - c.2744A>G likely benign r.(?) p.(Asn915Ser)
-?/. - c.2834T>C likely benign r.(?) p.(Met945Thr)
-?/. - c.3095T>C likely benign r.(?) p.(Ile1032Thr)
-?/. - c.3104G>T likely benign r.(?) p.(Gly1035Val)
-?/. - c.3130G>T likely benign r.(?) p.(Ala1044Ser)
?/. - c.3134G>C VUS r.(?) p.(Arg1045Thr)
-?/. - c.3377G>A likely benign r.(?) p.(Ser1126Asn)
-?/. - c.3661G>C likely benign r.(?) p.(Gly1221Arg)
-?/. - c.3679G>A likely benign r.(?) p.(Ala1227Thr)
-?/. - c.3860G>A likely benign r.(?) p.(Ser1287Asn)
?/. - c.4553C>T VUS r.(?) p.(Thr1518Met)
?/. - c.4766C>T VUS r.(?) p.(Ala1589Val)
?/. - c.4798G>A VUS r.(?) p.(Gly1600Arg)
-?/. - c.4859G>T likely benign r.(?) p.(Gly1620Val)
?/. - c.4996G>A VUS r.(?) p.(Ala1666Thr)
-?/. - c.5334G>A likely benign r.(?) p.(Met1778Ile)
-?/. - c.5417G>A likely benign r.(?) p.(Cys1806Tyr)
-?/. - c.5417G>A likely benign r.(?) p.(Cys1806Tyr)
-?/. - c.5441_5442insAGGCTC likely benign r.(?) p.(Gly1814_Ala1815insGlySer)
-?/. - c.5462C>T likely benign r.(?) p.(Ala1821Val)
?/. - c.5465A>G VUS r.(?) p.(Glu1822Gly)
-?/. - c.5490G>C likely benign r.(?) p.(Glu1830Asp)
?/. - c.5512G>A VUS r.(?) p.(Gly1838Arg)
-?/. - c.5560T>C likely benign r.(?) p.(Trp1854Arg)
?/. - c.6000G>T VUS r.(?) p.(Lys2000Asn)
-?/. - c.6012A>C likely benign r.(?) p.(Gln2004His)
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