Transcript #00014179 (NM_001080467.2, MYO5B gene)

Transcript name myosin VB
Gene name MYO5B (myosin VB)
Chromosome 18
Transcript - NCBI ID NM_001080467.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_001073936.1
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
+/. 40i c.? r.spl p.?
+/. 1 c.1A>G r.(?) p.0?
+/. 1 c.2T>A r.(?) p.(Met1?)
?/. - c.2T>C r.? p.?
+/. 1i c.27+2T>A r.spl? p.?
?/. 1i c.28-3C>A r.spl? p.?
+/. 1i c.28-2A>G r.spl p.?
+/. 1i_12i c.(27+1_28-1)_(1545+1_1546-1)del r.? p.?
+/. 2 c.42G>A r.(?) p.(Trp14*)
-?/. 3 c.160G>A r.(?) p.(Val54Ile)
-?/. - c.166C>T r.(?) p.(Arg56Cys)
-?/. 3 c.167G>T r.(?) p.(Arg56Leu)
-?/. - c.176T>C r.(?) p.(Leu59Pro)
-?/. 3 c.176T>C r.(?) p.(Leu59Pro)
-?/. - c.176T>C r.(?) p.(Leu59Pro)
?/. 3 c.183C>G r.(?) p.(Phe61Leu)
?/. - c.196G>T r.(?) p.(Asp66Tyr)
-?/. - c.207G>T r.(?) p.(Val69=)
?/. - c.290A>G r.(?) p.(Asn97Ser)
+/. 4 c.323T>G r.(?) p.(Val108Gly)
+/. - c.343C>T r.(?) p.(Gln115*)
-/. 4 c.376A>G r.(?) p.(Thr126Ala)
-/. 4 c.376A>G r.(?) p.(Thr126Ala)
+/. 4 c.428C>A r.(?) p.(Ala143Glu)
+/. 4 c.445C>T r.(?) p.(Gln149*)
+/. 4 c.445C>T r.(?) p.(Gln149*)
+/. 5 c.502G>A r.(?) p.(Gly168Arg)
?/. - c.541G>A r.(?) p.(Ala181Thr)
+/. 5 c.557C>A r.(?) p.(Ser186*)
?/. 6i c.655C>T r.(?) p.(Arg219Cys)
?/. - c.655C>T r.(?) p.(Arg219Cys)
?/. - c.655C>T r.(?) p.(Arg219Cys)
+/. 6 c.656G>A r.(?) p.(Arg219His)
+/. 6 c.656G>A r.(?) p.(Arg219His)
?/. - c.706G>A r.(?) p.(Gly236Arg)
-/. 6i c.756+6T>C r.(=) p.(=)
-?/. 7 c.780C>T r.(?) p.(His260=)
-?/. - c.864A>G r.(?) p.(Thr288=)
+/. 8 c.866C>A r.(?) p.(Ser289*)
+/. 8 c.871G>T r.(?) p.(Gly291Ter)
?/. - c.893G>A r.(?) p.(Gly298Asp)
-?/. - c.897G>T r.(?) p.(=)
-?/. 8 c.900C>T r.(?) p.(Asp300=)
-/. 8 c.921G>T r.(?) p.(Lys307Asn)
?/. 8 c.926G>A r.(?) p.(Arg309Gln)
+/. 8 c.946G>A r.(?) p.(Gly316Arg)
+/. 8 c.946G>A r.(?) p.(Gly316Arg)
+/. 8i c.947-1G>A r.spl p.?
+/. 9 c.947G>T r.(?) p.(Gly316Val)
-?/. 9 c.996C>A r.(?) p.(Ile332=)
+/. 9 c.1021C>T r.(?) p.(Gln341*)
?/. - c.1030C>T r.(?) p.(Arg344Cys)
?/. 9 c.1031G>A r.(?) p.(Arg344His)
-/. - c.1031G>A r.(?) p.(Arg344His)
-?/. 9i c.1057-4A>G r.spl? p.?
-?/. - c.1057-4A>G r.spl? p.?
+?/. - c.1064A>T r.(?) p.(Asp355Val)
+/. 10 c.1087C>T r.(?) p.(Arg363*)
?/. - c.1088G>A r.(?) p.(Arg363Gln)
+/. 10 c.1110_1113del r.(?) p.(Ser370Argfs*27)
?/. - c.1114A>T r.(?) p.(Met372Leu)
+/. 10 c.1125G>A r.(?) p.(Trp375*)
?/. - c.1135C>T r.(?) p.(Arg379Cys)
+?/. - c.1175T>C r.(?) p.(Met392Thr)
?/. - c.1201C>G r.(?) p.(Arg401Gly)
+/. 10 c.1202G>A r.(?) p.(Arg401His)
+/. 10 c.1202G>A r.(?) p.(Arg401His)
-/. 10 c.1206C>T r.(?) p.(Asn402=)
+/. 10 c.1222A>T r.(?) p.(Ile408Phe)
+/. 10 c.1222A>T r.(?) p.(Ile408Phe)
+/. 10 c.1303G>A r.(?) p.(Gly435Arg)
+?/. - c.1306G>T r.(?) p.(Val436Phe)
+/. 10i c.1323-2A>G r.spl p.?
+/. 10i c.1323-2A>G r.spl p.?
+/. 11 c.1347del r.(?) p.(Phe450Leufs*30)
+/. 11 c.1347del r.(?) p.(Phe450Leufs*30)
+/. - c.1355A>G r.(?) p.(Gln452Arg)
+/. 11 c.1355_1363dup r.(?) p.(Cys454_Ile455insLysPheCys)
+/. 11 c.1367A>G r.(?) p.(Asn456Ser)
?/. 11 c.1404G>A r.(?) p.(Ser468=)
?/. - c.1406del r.(?) p.(His469Leufs*11)
?/. - c.1445A>G r.(?) p.(Gln482Arg)
+?/. 12i c.1526T>C r.(?) p.(Leu509Pro)
+/. 12 c.1540T>C r.(?) p.(Cys514Arg)
-/. 12i c.1545+11T>C r.(=) p.(=)
-/. 12i c.1545+11T>C r.(=) p.(=)
?/. - c.1546G>A r.(?) p.(Val516Ile)
?/. - c.1578G>A r.(?) p.(Gln526=)
+/. 13 c.1582C>T r.(?) p.(Leu528Phe)
+/. 13 c.1582C>T r.(?) p.(Leu528Phe)
+/. 13 c.1591C>T r.(?) p.(Arg531Trp)
+/. 13 c.1613T>C r.(?) p.(Phe538Ser)
+/. 13 c.1648A>T r.(?) p.(Ile550Phe)
?/. - c.1679T>G r.(?) p.(Leu560Arg)
-?/. - c.1713G>C r.(?) p.(Thr571=)
-?/. - c.1793C>T r.(?) p.(Pro598Leu)
+/. 15 c.1856C>T r.(?) p.(Pro619Leu)
+/. 15i c.1906-1G>A r.spl p.?
?/. - c.1954C>G r.(?) p.(Pro652Ala)
+?/. - c.1966C>A r.(?) p.(Arg656Ser)
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