Transcript #00003475 (NM_004333.4, BRAF gene)

Transcript name v-raf murine sarcoma viral oncogene homolog B1
Gene name BRAF (v-raf murine sarcoma viral oncogene homolog B1)
Chromosome 7
Transcript - NCBI ID NM_004333.4
Transcript - Ensembl ID -
Protein - NCBI ID NP_004324.2
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 0000-00-00 00:00:00 +00:19 (LMT)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-5A>G r.(?) p.(=)
-?/. - c.36G>A r.(?) p.(Ala12=)
-?/. - c.41C>T r.(?) p.(Pro14Leu)
?/. - c.64G>A r.(?) p.(Asp22Asn)
?/. - c.64G>A r.(?) p.(Asp22Asn)
-/. - c.78G>T r.(?) p.(Glu26Asp)
-/. - c.78G>T r.(?) p.(Glu26Asp)
-?/. - c.78G>T r.(?) p.(Glu26Asp)
?/. - c.89_100del r.(?) p.(Gly30_Ala33del)
-?/. - c.95_100del r.(?) p.(Gly32_Ala33del)
-?/. - c.95_100dup r.(?) p.(Gly32_Ala33dup)
?/. - c.113C>T r.(?) p.(Ala38Val)
-?/. - c.139-12A>C r.(=) p.(=)
?/. - c.181A>G r.(?) p.(Ile61Val)
?/. - c.205G>A r.(?) p.(Gly69Ser)
-?/. - c.240+18A>G r.(=) p.(=)
?/. - c.261C>G r.(?) p.(Ser87Arg)
-?/. - c.357C>T r.(?) p.(Thr119=)
-?/. - c.357C>T r.(?) p.(Thr119=)
?/. - c.368C>T r.(?) p.(Ser123Phe)
?/. - c.394C>T r.(?) p.(Pro132Ser)
?/. - c.608+4T>C r.spl? p.?
-?/. - c.608+19G>C r.(=) p.(=)
?/. - c.609-5T>C r.spl? p.?
-?/. - c.708C>T r.(?) p.(Asn236=)
+/. - c.721A>C r.(?) p.(Thr241Pro)
+/. - c.722C>T r.(?) p.(Thr241Met)
+/. - c.722C>T r.(?) p.(Thr241Met)
+?/. - c.741T>G r.(?) p.(Phe247Leu)
+/. - c.769C>A r.(?) p.(Gln257Lys)
+/. - c.770A>G r.(?) p.(Gln257Arg)
+/. - c.770A>G r.(?) p.(Gln257Arg)
+/. - c.770A>G r.(?) p.(Gln257Arg)
+?/. 6 c.770A>G r.?= p.(Gln257Arg)
?/. - c.778C>G r.(?) p.(Arg260Gly)
+?/. - c.785A>C r.(?) p.(Gln262Pro)
+?/. - c.793G>C r.(?) p.(Gly265Arg)
-?/. - c.837G>A r.(?) p.(Met279Ile)
?/. - c.837G>A r.(?) p.(Met279Ile)
?/. - c.866T>A r.(?) p.(Leu289Gln)
?/. - c.900A>C r.(=) p.(=)
+?/. - c.980+1G>A r.spl? p.?
-?/. - c.1002G>A r.(?) p.(Pro334=)
?/. - c.1021C>G r.(?) p.(Pro341Ala)
?/. - c.1024A>G r.(?) p.(Ile342Val)
-?/. - c.1024A>G r.(?) p.(Ile342Val)
?/. - c.1039C>T r.(?) p.(Arg347*)
?/. - c.1058A>G r.(?) p.His353Arg
-?/. - c.1068A>G r.(?) p.(Gln356=)
+?/. - c.1085G>A r.(?) p.(Arg362Gln)
?/. - c.1122A>G r.(?) p.(Ile374Met)
?/. - c.1140+2T>A r.spl? p.?
-/. - c.1141-19C>T r.(=) p.(=)
?/. - c.1141G>A r.(?) p.(Asp381Asn)
?/. - c.1141G>A r.(?) p.(Asp381Asn)
-?/. - c.1150A>G r.(?) p.(Arg384Gly)
-?/. - c.1165C>T r.(?) p.(Arg389Cys)
-?/. - c.1165C>T r.(?) p.(Arg389Cys)
-?/. - c.1205C>A r.(?) p.(Pro402His)
-?/. - c.1227A>G r.(?) p.(Ser409=)
-/. - c.1227A>G r.(?) p.(Ser409=)
?/. - c.1271G>A r.(?) p.(Arg424Gln)
-/. - c.1315-18T>G r.(=) p.(=)
-/. - c.1315-18T>G r.(=) p.(=)
-?/. - c.1332G>A r.(?) p.(Arg444=)
-/. - c.1383A>G r.(?) p.(Gln461=)
-/. - c.1383A>G r.(?) p.(Gln461=)
+/. - c.1390G>A r.(?) p.(Gly464Arg)
+?/. - c.1391G>C r.(?) p.(Gly464Ala)
+/. - c.1391G>T r.(?) p.(Gly464Val)
+/. - c.1403T>C r.(?) p.(Phe468Ser)
+/. - c.1405G>A r.(?) p.(Gly469Arg)
+/. 11 c.1406G>A r.(?) p.(Gly469Glu)
+/. - c.1406G>C r.(?) p.(Gly469Ala)
+/. 11 c.1411G>T r.(?) p.(Val471Phe)
-?/. - c.1429C>T r.(?) p.(His477Tyr)
-?/. - c.1433-19A>G r.(=) p.(=)
-?/. - c.1433-19A>G r.(=) p.(=)
+?/. - c.1442C>A r.(?) p.(Ala481Glu)
+?/. - c.1449A>T r.(?) p.(Lys483Asn)
+/. - c.1460T>G r.(?) p.(Val487Gly)
?/. - c.1478A>G r.(?) p.(Gln493Arg)
?/. - c.1490C>T r.(?) p.(Ala497Val)
+/. - c.1495A>G r.(?) p.(Lys499Glu)
+/. - c.1497A>C r.(?) p.(Lys499Asn)
+?/. - c.1502A>G r.(?) p.(Glu501Gly)
?/. - c.1505T>A r.(?) p.(Val502Glu)
+/. - c.1513C>T r.(?) p.(Leu505Phe)
-?/. - c.1518-7T>C r.(=) p.(=)
+?/. - c.1518_1526dup r.(?) p.(Lys507_Arg509dup)
+?/. - c.1525C>T r.(?) p.(Arg509*)
?/. - c.1591T>C r.(?) p.(Trp531Arg)
./. - c.1595G>A r.(?) p.(Cys532Tyr)
?/. - c.1627A>G r.(?) p.(Ile543Val)
?/. - c.1657C>T r.(?) p.(Leu553Phe)
?/. - c.1673G>A r.(?) p.(Arg558Gln)
?/. - c.1685A>T r.(?) p.(Gln562Leu)
-?/. - c.1694+14G>A r.(=) p.(=)
+?/. 14 c.1695T>A r.(?) p.(Asp565Glu)
+?/. 14 c.1722C>G r.(?) p.(His574Gln)
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