Transcript #00013652 (NM_198159.2, MITF gene)

Transcript name transcript variant 1
Gene name MITF (microphthalmia-associated transcription factor)
Chromosome 3
Transcript - NCBI ID NM_198159.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_937802.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+?/? _1_1i c.?_(105-12864_?)dup r.? p.?
+/+ _1_10_ c.?_(1291_?)del r.? p.?
+/+ _1_10_ c.?_(1291_?)del r.0? p.0?
+/+ _1_10_ c.0 r.0? p.0?
-?/. - c.38T>C r.(?) p.(Val13Ala)
?/. - c.104+24168G>C r.(=) p.(=)
-?/. - c.104+24208C>T r.(=) p.(=)
-?/. - c.104+24216T>C r.(=) p.(=)
-/. - c.104+24216T>C r.(=) p.(=)
-?/. - c.104+24226G>A r.(=) p.(=)
-?/. - c.105-12813C>T r.(=) p.(=)
?/. - c.107G>T r.(?) p.(Ser36Ile)
?/. - c.118C>T r.(?) p.(His40Tyr)
?/. - c.319C>T r.(?) p.(Pro107Ser)
?/. - c.329C>T r.(?) p.(Thr110Met)
-/. - c.330G>A r.(?) p.(Thr110=)
-?/. - c.345A>G r.(?) p.(Glu115=)
+/+ 2i c.355-1080A>G r.(=) p.(=)
-?/? 2i c.355-1080A>G r.? p.?
+?/? 2i c.355-1072T>A r.? p.?
+/+ 2i c.355-1066G>A r.? p.?
+/+ 2i c.355-1066G>A r.? p.?
+?/+? 2i c.355-1062G>C r.? p.?
-?/. - c.355-1061_355-1055del r.(?) p.(=)
-?/. - c.366C>T r.(?) p.(His122=)
-/. - c.366C>T r.(?) p.(His122=)
?/. - c.366C>T r.(?) p.(His122=)
+/. - c.383dup r.(?) p.(Tyr129ValfsTer22)
?/. - c.400G>A r.(?) p.(Ala134Thr)
?/. - c.452A>C r.(?) p.(His151Pro)
-?/. - c.475C>T r.(?) p.(Pro159Ser)
-?/. - c.519G>A r.(?) p.(Pro173=)
-/. - c.582+22_582+26dup r.(=) p.(=)
-?/. - c.639C>T r.(?) p.(Asn213=)
+?/. - c.644dup r.(?) p.(His215Glnfs*11)
+/+ 4 c.649C>T r.(?) p.(Arg217*)
+/. - c.649C>T r.(?) p.(Arg217Ter)
+?/. 7 c.649del r.(?) p.(Arg217Glufs*10)
-?/-? 4 c.653C>T r.(?) p.(Ala218Val)
?/. - c.653C>T r.(?) p.(Ala218Val)
-?/. - c.666+8A>G r.(=) p.(=)
-?/. - c.666+15G>C r.(=) p.(=)
-?/. - c.666+22T>C r.(=) p.(=)
+/+ 5i c.732del r.(?) p.(Met245Trpfs*17)
-?/-? 5 c.736G>A r.(?) p.(Asp246Asn)
+/+ 5i c.763-2A>C r.spl? p.?
+/+ 5i c.763-2A>C r.spl? p.?
+/. - c.763-2A>G r.spl? p.?
+/+ 5i c.763-1G>C r.763_880del p.Leu255Serfs*19
-?/. - c.771C>A r.(?) p.(Val257=)
+/. - c.787del r.(?) p.(Asp263Ilefs*26)
?/. - c.794A>G r.(?) p.(Tyr265Cys)
-?/-? 6 c.804A>T r.(?) p.(Gln268His)
-?/. - c.804A>T r.(?) p.(Gln268His)
-?/. - c.836A>G r.(?) p.(Asn279Ser)
-?/. - c.880+9C>G r.(=) p.(=)
-?/. - c.880+9C>G r.(=) p.(=)
-/. - c.880+9C>G r.(=) p.(=)
-/. - c.881-25T>A r.(=) p.(=)
+/+ 6i c.881-3del r.spl? p.?
+/+ 6i c.881-3del r.spl? p.?
-?/. - c.882G>A r.(?) p.(Glu294=)
+/+ 6 c.882_883del r.(?) p.(Glu294Aspfs*2)
-?/-? 7 c.911G>A r.(?) p.(Arg304Lys)
+?/+? 7 c.919A>C r.(?) p.(Lys307Gln)
+/. 7 c.921G>C r.(?) p.(Lys307Asn)
+/. 7 c.921G>C r.(?) p.(Lys307Asn)
+?/+? 7 c.928C>T r.(?) p.(His310Tyr)
+?/. - c.929A>T r.(?) p.(His310Leu)
+/+ 7 c.933C>G r.(?) p.(Asn311Lys)
+?/+? 7 c.933C>G r.(?) p.(Asn311Lys)
+/+ 7i c.937+1G>A r.spl? p.?
+/+ 7i c.937+1G>A r.spl p.?
+/. 7i c.938-1G>A r.spl p.?
+/. 7i c.938-1G>A r.spl p.?
+/. - c.938-1G>A r.spl p.?
+?/+? 8 c.938T>G r.(?) p.(Ile313Ser)
+/+ 8 c.939T>G r.(?) p.(Ile313Met)
+/. - c.940G>T r.(?) p.(Glu314Ter)
+?/+? 8 c.942A>C r.(?) p.(Glu314Asp)
+/+ 8 c.942del r.(?) p.(Glu314Aspfs*8)
+/+ 8 c.943C>T r.(?) p.(Arg315*)
+/+ 8 c.943C>T r.(?) p.(Arg315*)
+/+ 8 c.943C>T r.(?) p.(Arg315*)
+/. - c.943C>T r.(?) p.(Arg315Ter)
+?/+? 8 c.950G>A r.(?) p.(Arg317Lys)
+/. 8 c.952A>G r.(?) p.(Arg318Gly)
+/. 8 c.952A>G r.(?) p.(Arg318Gly)
+/+ 8 c.952A>G r.(?) p.(Arg318Gly)
+?/+? 8 c.952A>G r.(?) p.(Arg318Gly)
+/. 8 c.952_954del r.(?) p.(Arg318del)
+/. 8 c.952_954del r.(?) p.(Arg318del)
+?/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
+/+ 8 c.952_954del r.(?) p.(Arg318del)
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