Transcript #00002741

Transcript name transcript variant 2
Gene name ARAF (v-raf murine sarcoma 3611 viral oncogene homolog)
Chromosome X
Transcript - NCBI ID NM_001256196.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001243125.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -


Variants

69 entries on 1 page. Showing entries 1 - 69.
Legend  

Affects function     

Exon     

AscendingDNA change (cDNA)     

ClassClinical     

RNA change     

Protein     
?/. - c.44C>T VUS r.(?) p.(Ser15Phe)
?/. - c.59C>T VUS r.(?) p.(Thr20Ile)
-?/. - c.201-3C>T likely benign r.spl? p.?
-?/. - c.449A>G likely benign r.(?) p.(Asn150Ser)
-?/. - c.465A>G likely benign r.(?) p.(=)
?/. - c.551C>A - r.(?) p.(Thr184Asn)
?/. - c.633G>C VUS r.(?) p.(Gln211His)
-?/. - c.736+8C>A likely benign r.(=) p.(=)
-?/. - c.794G>T likely benign r.(?) p.(Ser265Ile)
-?/. - c.814T>G likely benign r.(?) p.(Ser272Ala)
?/. - c.1019T>C VUS r.(?) p.(Val340Ala)
?/. - c.1027G>A VUS r.(?) p.(Val343Met)
-?/. - c.1787A>C likely benign r.(?) p.(Glu596Ala)
-?/. - c.*1296G>A likely benign r.(=) p.(=)
-/. - c.*1359G>T benign r.(=) p.(=)
-?/. - c.*1529G>A likely benign r.(=) p.(=)
-?/. - c.*2589T>G likely benign r.(=) p.(=)
-/. - c.*2828T>C benign r.(=) p.(=)
-?/. - c.*2828T>C likely benign r.(=) p.(=)
-?/. - c.*2828T>C likely benign r.(=) p.(=)
?/. - c.*2867G>A VUS r.(=) p.(=)
-?/. - c.*2898A>G likely benign r.(=) p.(=)
-?/. - c.*2912C>T likely benign r.(=) p.(=)
-?/. - c.*2912C>T likely benign r.(=) p.(=)
-?/. - c.*3089G>A likely benign r.(=) p.(=)
-?/. - c.*3299A>G likely benign r.(=) p.(=)
-?/. - c.*3557G>A likely benign r.(=) p.(=)
+/. - c.*3712G>A pathogenic r.(=) p.(=)
-?/. - c.*3824G>A likely benign r.(=) p.(=)
-?/. - c.*4725G>A likely benign r.(=) p.(=)
-?/. - c.*4725G>A likely benign r.(=) p.(=)
-?/. - c.*4785_*4791del likely benign r.(=) p.(=)
-?/. - c.*5027G>A likely benign r.(=) p.(=)
-?/. - c.*5077C>T likely benign r.(=) p.(=)
-?/. - c.*5317C>T likely benign r.(=) p.(=)
?/. - c.*13505C>T VUS r.(=) p.(=)
-?/. - c.*13505C>T likely benign r.(=) p.(=)
-?/. - c.*13552G>T likely benign r.(=) p.(=)
-?/. - c.*14067G>A likely benign r.(=) p.(=)
-?/. - c.*14082T>A likely benign r.(=) p.(=)
-?/. - c.*14165C>G likely benign r.(=) p.(=)
-?/. - c.*14441C>T likely benign r.(=) p.(=)
-?/. - c.*15122C>T likely benign r.(=) p.(=)
-?/. - c.*15164G>A likely benign r.(=) p.(=)
?/. - c.*15184C>T VUS r.(=) p.(=)
-?/. - c.*15185G>A likely benign r.(=) p.(=)
-?/. - c.*15221C>T likely benign r.(=) p.(=)
+?/. - c.*33595G>A likely pathogenic r.(=) p.(=)
-?/. - c.*33706A>G likely benign r.(=) p.(=)
?/. - c.*33787G>T VUS r.(=) p.(=)
-?/. - c.*33851C>T likely benign r.(=) p.(=)
?/. - c.*33869C>T VUS r.(=) p.(=)
?/. - c.*33870G>A VUS r.(=) p.(=)
?/. - c.*33870G>A VUS r.(=) p.(=)
?/. - c.*33870G>A VUS r.(=) p.(=)
-?/. - c.*33870G>A likely benign r.(=) p.(=)
?/. - c.*33870G>A VUS r.(=) p.(=)
-/. - c.*35505A>G benign r.(=) p.(=)
-?/. - c.*35543T>G likely benign r.(=) p.(=)
-?/. - c.*35543T>G likely benign r.(=) p.(=)
-?/. - c.*35565A>C likely benign r.(=) p.(=)
-?/. - c.*35565A>C likely benign r.(=) p.(=)
-?/. - c.*35693T>C likely benign r.(=) p.(=)
-?/. - c.*35693T>C likely benign r.(=) p.(=)
-?/. - c.*47908G>A likely benign r.(=) p.(=)
-?/. - c.*48083C>A likely benign r.(=) p.(=)
-?/. - c.*48299G>C likely benign r.(=) p.(=)
-?/. - c.*48352A>G likely benign r.(=) p.(=)
-/. - c.*52944G>A benign r.(=) p.(=)
Legend