Transcript #00014134 (NM_017534.5, MYH2 gene)

Transcript name transcript variant 1
Gene name MYH2 (myosin, heavy chain 2, skeletal muscle, adult)
Chromosome 17
Transcript - NCBI ID NM_017534.5
Transcript - Ensembl ID -
Protein - NCBI ID NP_060004.3
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

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-126A>G r.(=) p.(=)
-?/. - c.-126A>G r.(=) p.(=)
+?/. _3_14i c.(?_1)_(1416+1_1417-1)del r.0? p.0?
?/. - c.41C>T r.(?) p.(Ala14Val)
?/. - c.182C>T r.(?) p.Thr61Met
-/. - c.183G>A r.(?) p.(Thr61=)
-/. - c.183G>A r.(?) p.(Thr61=)
-?/. - c.193G>C r.(?) p.(Glu65Gln)
?/. 3 c.200G>A r.(?) p.(Gly67Glu)
-/. - c.324A>G r.(?) p.(Glu108=)
-/. - c.324A>G r.(?) p.(Glu108=)
-/. - c.324A>G r.(?) p.(Glu108=)
?/. - c.332C>T r.(?) p.(Ala111Val)
-?/. - c.332C>T r.(?) p.(Ala111Val)
-/. - c.399T>A r.(?) p.(Pro133=)
-/. - c.399T>A r.(?) p.(Pro133=)
-/. - c.399T>A r.(?) p.(Pro133=)
?/. - c.680A>T r.(?) p.(Asn227Ile)
+/. - c.685del r.(?) p.(Leu229TyrfsTer11)
-?/. - c.805+8T>A r.(=) p.(=)
+/+ 10i c.904+1G>A r.806_904del p.Tyr269Ter
+/+ 10i c.904+1G>A r.806_904del p.Tyr269Ter
+/+ 10i c.904+1G>A r.806_904del p.Tyr269Ter
-/. - c.904+10G>A r.(=) p.(=)
-/. - c.904+10G>A r.(=) p.(=)
-/. - c.904+10G>A r.(=) p.(=)
?/. - c.1072G>T r.(?) p.(Ala358Ser)
?/. - c.1160C>T r.(?) p.(Ala387Val)
+?/. - c.1160C>T r.(?) p.(Ala387Val)
?/. - c.1289T>G r.(?) p.(Leu430Arg)
?/. - c.1306G>A r.(?) p.(Glu436Lys)
?/. - c.1334G>T r.(?) p.(Arg445Leu)
?/. - c.1381G>A r.(?) p.(Gly461Arg)
+?/. - c.1417-2A>C r.spl? p.?
+?/. - c.1417-1G>C r.spl? p.?
-?/. - c.1587+16C>T r.(=) p.(=)
+/. - c.1920del r.(?) p.(Gly642ValfsTer20)
+/. - c.1920del r.(?) p.(Gly642ValfsTer20)
-/. - c.1975-9G>A r.(=) p.(=)
-/. - c.1975-9G>A r.(=) p.(=)
+/+ 17i c.1975-2A>G r.1975_2062del p.Glu659ValfsTer12
+/+ 17i c.1975-2A>G r.1975_2062del p.Glu659ValfsTer12
-/. - c.2062+8A>G r.(=) p.(=)
+?/. - c.2063-2A>T r.spl p.?
?/. 19 c.2075A>G r.(?) p.(His692Arg)
?/. - c.2092C>G r.(?) p.(Gln698Glu)
?/. - c.2096T>C r.(?) p.Leu699Pro
+/+ 17 c.2116G>A r.(?) p.(Glu706Lys)
?/. - c.2266G>A r.(?) p.(Asp756Asn)
?/. - c.2270T>C r.(?) p.(Ile757Thr)
?/. - c.2270T>C r.(?) p.(Ile757Thr)
+/+ 21 c.2347C>T r.2347c>u p.Arg783Ter
+/+ 21 c.2347C>T r.2347c>u p.Arg783Ter
+/+ 21 c.2347C>T r.2347c>u p.Arg783Ter
+/+ 21 c.2347C>T r.2347c>u p.Arg783Ter
+?/. 21 c.2377C>T r.(?) p.(Arg793Ter)
+/+ 21 c.2400del r.(?) p.(Phe801Serfs*28)
+/+ 21 c.2400del r.(?) p.(Phe801Serfs*28)
+/+ 21 c.2400del r.(?) p.(Phe801Serfs*28)
+/+ 21 c.2400del r.0 p.0
+/+ 21 c.2400del r.(?) p.(Phe801Serfs*28)
+/+ 21 c.2400del r.(?) p.(Phe801Serfs*28)
+/+ 21 c.2400del r.0 p.0
+/+ 21 c.2405T>A r.2533u>a p.Leu802Ter
+/+ 21 c.2405T>A r.2533u>a p.Leu802Ter
+/. - c.2414T>C r.(?) p.(Val805Ala)
+?/. - c.2615C>G r.(?) p.(Ser872Ter)
+?/. - c.2615C>G r.(?) p.(Ser872Ter)
?/. - c.2697+6T>A r.(=) p.(=)
?/. - c.2728A>G r.(?) p.(Arg910Gly)
-?/. - c.2889T>C r.(?) p.(Leu963=)
-?/. - c.2908G>A r.(?) p.(Val970Ile)
-?/. - c.2908G>A r.(?) p.(Val970Ile)
+?/. - c.2927C>T r.(?) p.(Ala976Val)
?/. - c.2965G>A r.(?) p.(Ala989Thr)
+?/. - c.3117+1G>A r.spl? p.?
-?/. - c.3127T>G r.(?) p.(Ser1043Ala)
-?/. - c.3127T>G r.(?) p.(Ser1043Ala)
?/. - c.3127T>G r.(?) p.(Ser1043Ala)
-?/. - c.3181C>G r.(?) p.(Leu1061Val)
-?/. - c.3181C>G r.(?) p.(Leu1061Val)
-?/. - c.3181C>G r.(?) p.(Leu1061Val)
?/. - c.3263+11_3263+12del r.(=) p.(=)
-?/. - c.3263+14_3263+15del r.(=) p.(=)
-/. - c.3263+15A>G r.(=) p.(=)
-/. - c.3263+15A>G r.(=) p.(=)
?/. - c.3334A>G r.(?) p.(Lys1112Glu)
?/. - c.3362T>C r.(?) p.(Ile1121Thr)
-?/. - c.3384C>T r.(?) p.(Ile1128=)
?/. - c.3403C>T r.(?) p.(Arg1135Trp)
-?/. - c.3432C>T r.(?) p.(Asp1144=)
+?/. - c.3469G>A r.(?) p.(Glu1157Lys)
?/. - c.3553G>A r.(?) p.(Glu1185Lys)
-/. - c.3582A>G r.(?) p.(=)
?/. - c.3622G>A r.(?) p.(Glu1208Lys)
-?/. - c.3709C>T r.(?) p.(Leu1237Phe)
-?/. - c.3872-16T>C r.(=) p.(=)
?/. - c.3884G>A r.(?) p.(Arg1295His)
-?/. - c.4007C>A r.(?) p.(Ala1336Glu)
?/. 30 c.4027C>G r.(?) p.(Arg1343Gly)
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