Transcript #00000023 (NM_000259.3, MYO5A gene)

Transcript name myosin VA (heavy chain 12, myoxin), transcript variant 1
Gene name MYO5A (myosin VA (heavy chain 12, myoxin))
Chromosome 15
Transcript - NCBI ID NM_000259.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_000250.3
Protein - Ensembl ID -
Protein - Uniprot ID -
Remarks -
Date created 2012-05-11 13:11:51 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.27+9C>T r.(=) p.(=)
?/. - c.40T>G r.(?) p.(Trp14Gly)
-?/. - c.169A>G r.(?) p.(Lys57Glu)
-?/. - c.207T>C r.(?) p.(Val69=)
?/. - c.290A>G r.(?) p.(Lys97Arg)
-?/. - c.290A>G r.(?) p.(Lys97Arg)
-?/. - c.696T>C r.(?) p.(Tyr232=)
-?/. - c.839-7A>G r.(=) p.(=)
-/. - c.839-7A>G r.(=) p.(=)
?/. - c.989C>T r.(?) p.(Ala330Val)
?/. - c.1020T>A r.(?) p.(Phe340Leu)
-/. - c.1029A>C r.(?) p.(Arg343=)
?/. - c.1058A>G r.(?) p.(Lys353Arg)
-/. - c.1086= r.(=) p.(Asp362=)
?/. - c.1132C>T r.(?) p.(Arg378Trp)
?/. - c.1157C>A r.(?) p.(Thr386Lys)
?/. - c.1190C>T r.(?) p.(Thr397Met)
-/. - c.1191= r.(=) p.(Thr397=)
?/. - c.1259A>G r.(?) p.(Asn420Ser)
-?/. - c.1368T>C r.(?) p.(Tyr456=)
-?/. - c.1368T>C r.(?) p.(Tyr456=)
-?/. - c.1543-14_1543-13delinsC r.(=) p.(=)
-/. - c.1543-13T>C r.(=) p.(=)
?/. - c.1543-6A>G r.(=) p.(=)
?/. - c.1639G>A r.(?) p.(Ala547Thr)
-/. - c.1753-18A>G r.(=) p.(=)
-?/. - c.1764A>G r.(?) p.(Leu588=)
-?/. - c.1880T>C r.(?) p.(Met627Thr)
-/. - c.2012+17C>T r.(=) p.(=)
-?/. - c.2067C>G r.(?) p.(Thr689=)
-?/. - c.2067C>G r.(?) p.(Thr689=)
-?/. - c.2082G>A r.(?) p.(Ala694=)
-?/. - c.2082G>A r.(?) p.(Ala694=)
-/. - c.2085C>T r.(?) p.(Ala695=)
-?/. - c.2099+10G>A r.(=) p.(=)
-?/. - c.2329A>C r.(?) p.(Ile777Leu)
./. - c.2437C>T r.(?) p.(Arg813Cys)
?/. - c.2438G>A r.(?) p.(Arg813His)
-/. - c.2526= r.(=) p.(Ile842=)
-/. - c.2541C>T r.(?) p.(Tyr847=)
?/. - c.2576A>G r.(?) p.(Lys859Arg)
?/. - c.2584C>T r.(?) p.(Arg862Cys)
-?/. - c.2585G>A r.(?) p.(Arg862His)
?/. - c.2621G>A r.(?) p.(Arg874Gln)
?/. - c.2660A>G r.(?) p.(His887Arg)
?/. - c.2707C>T r.(?) p.(Arg903Cys)
-/. - c.2814G>A r.(?) p.(Glu938=)
-?/. - c.3131G>A r.(?) p.(Arg1044His)
-?/. - c.3136G>A r.(?) p.(Val1046Met)
?/. - c.3191C>T r.(?) p.(Thr1064Met)
-/. - c.3309+18G>T r.(=) p.(=)
?/. - c.3358_3360del r.(?) p.(Asn1120del)
?/. - c.3422A>T r.(?) p.(Glu1141Val)
?/. - c.3481C>T r.(?) p.(Arg1161Trp)
-?/. - c.3567+19C>T r.(=) p.(=)
-/. - c.3567+19C>T r.(=) p.(=)
-?/. - c.3568-4C>T r.spl? p.?
-?/. - c.3568-4C>T r.spl? p.?
?/. - c.3620A>G r.(?) p.(Lys1207Arg)
-/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
?/. - c.3736C>T r.(?) p.(Arg1246Cys)
-/. - c.3849+7G>A r.(=) p.(=)
?/. - c.3850-2A>G r.spl? p.?
-?/. - c.3858+9A>T r.(=) p.(=)
-?/. - c.3866T>C r.(?) p.(Met1289Thr)
-/. - c.3959+8G>A r.(=) p.(=)
-?/. - c.3993G>A r.(?) p.(Glu1331=)
-/. - c.4041-11C>G r.(=) p.(=)
?/. - c.4041G>T r.(?) p.(Arg1347Ser)
?/. - c.4097C>T r.(?) p.(Ala1366Val)
-?/. - c.4158C>G r.(?) p.(Ala1386=)
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