Transcript #00025323 (NM_001145809.1, MYH14 gene)

Transcript name transcript variant 3
Gene name MYH14 (myosin, heavy chain 14, non-muscle)
Chromosome 19
Transcript - NCBI ID NM_001145809.1
Transcript - Ensembl ID -
Protein - NCBI ID NP_001139281.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2018-10-09 17:14:48 +02:00 (CEST)
Date last edited N/A


Variants

291 entries on 3 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-3-269C>A r.(=) p.(=)
-/. - c.33G>C r.(?) p.(Arg11=)
-/. - c.33G>C r.(?) p.(Arg11=)
-?/. - c.36G>A r.(?) p.(Lys12=)
?/. - c.64G>A r.(?) p.(Glu22Lys)
+/. 2 c.73C>T r.(?) p.(Gln25*)
-/. - c.91C>A r.(?) p.(Pro31Thr)
?/. - c.95G>A r.(?) p.(Arg32His)
?/. - c.169_173del r.(?) p.(Trp57AlafsTer132)
?/. - c.173_174insAA r.(?) p.(Pro59SerfsTer42)
-/. - c.192G>T r.(?) p.(Gly64=)
-/. - c.192G>T r.(?) p.(Gly64=)
?/. - c.263G>C r.(?) p.(Arg88Pro)
+?/. - c.359C>T r.(?) p.(Ser120Leu)
?/. - c.371A>G r.(?) p.(Asn124Ser)
-?/. - c.394G>A r.(?) p.(Gly132Ser)
-?/. - c.394G>A r.(?) p.(Gly132Ser)
-?/. - c.420T>C r.(?) p.(Leu140=)
-/. - c.474T>C r.(?) p.(Ile158=)
-?/. - c.483G>A r.(?) p.(Met161Ile)
-?/. - c.483G>A r.(?) p.(Met161Ile)
-?/. - c.483G>A r.(?) p.(Met161Ile)
-?/. - c.525C>T r.(?) p.(Tyr175=)
-?/. - c.526G>A r.(?) p.(Ala176Thr)
?/. - c.539G>A r.(?) p.(Gly180Glu)
?/. - c.548G>A r.(?) p.(Arg183Gln)
?/. - c.560A>G r.(?) p.(Gln187Arg)
-/. - c.563-21C>G r.(=) p.(=)
-?/. - c.565C>T r.(?) p.(Arg189Cys)
?/. - c.565C>T r.(?) p.(Arg189Cys)
+?/. 4 c.572A>G r.(?) p.(Asp191Gly)
-/. - c.657G>A r.(?) p.(Ala219=)
-/. - c.657G>A r.(?) p.(Ala219=)
-?/. - c.693+12C>T r.(=) p.(=)
-/. - c.694-20G>A r.(=) p.(=)
-?/. - c.699C>A r.(?) p.(Ser233=)
?/. - c.727G>C r.(?) p.(Glu243Gln)
?/. - c.731G>A r.(?) p.(Arg244Gln)
?/. - c.752C>A r.(?) p.(Pro251His)
?/. - c.752C>A r.(?) p.(Pro251His)
-?/. - c.783A>G r.(?) p.(Thr261=)
?/. - c.793G>A r.(?) p.(Asp265Asn)
-/. - c.810+21G>A r.(=) p.(=)
-?/. - c.818T>C r.(?) p.(Phe273Ser)
?/. - c.820A>G r.(?) p.(Ile274Val)
?/. - c.820A>G r.(?) p.(Ile274Val)
-?/. - c.826A>G r.(?) p.(Ile276Val)
-?/. - c.838G>A r.(?) p.(Val280Ile)
?/. - c.838G>A r.(?) p.(Val280Ile)
?/. - c.863A>G r.(?) p.(Asn288Ser)
-?/. - c.866T>C r.(?) p.(Ile289Thr)
-?/. - c.973+5G>A r.spl? p.?
-?/. - c.984C>T r.(?) p.(Leu328=)
?/. - c.1003T>C r.(?) p.(Tyr335His)
+/. - c.1067C>T r.(?) p.(Thr356Met)
?/. - c.1067C>T r.(?) p.(Thr356Met)
-/. - c.1114+13C>T r.(=) p.(=)
-/. - c.1114+13C>T r.(=) p.(=)
-?/. - c.1115-4C>T r.spl? p.?
-?/. - c.1120C>T r.(?) p.(Leu374=)
-?/. - c.1125G>T r.(?) p.(Arg375=)
-/. - c.1149T>C r.(?) p.(Phe383=)
-?/. - c.1150G>T r.(?) p.(Gly384Cys)
-?/. - c.1150G>T r.(?) p.(Gly384Cys)
-?/. - c.1150G>T r.(?) p.(Gly384Cys)
-?/. - c.1174C>T r.(?) p.(Arg392Trp)
-?/. - c.1205A>G r.(?) p.(Asn402Ser)
?/. - c.1244G>A r.(?) p.(Gly415Glu)
?/. - c.1265C>G r.(?) p.(Ala422Gly)
+?/. - c.1306C>T r.(?) p.(Gln436*)
-/. - c.1329+15C>T r.(=) p.(=)
-/. - c.1329+16G>A r.(=) p.(=)
?/. - c.1339G>A r.(?) p.(Ala447Thr)
-?/. - c.1368C>T r.(?) p.(Tyr456=)
?/. - c.1373G>A r.(?) p.(Arg458His)
-?/. - c.1382G>T r.(?) p.(Arg461Leu)
?/. - c.1418G>A r.(?) p.(Arg473His)
-?/. - c.1419C>T r.(?) p.(Arg473=)
-?/. - c.1419C>T r.(?) p.(Arg473=)
?/. - c.1466G>A r.(?) p.(Gly489Asp)
-/. - c.1483-10G>A r.(=) p.(=)
?/. - c.1621G>A r.(?) p.(Asp541Asn)
-?/. - c.1652G>A r.(?) p.(Arg551Gln)
-?/. - c.1707G>C r.(?) p.(Pro569=)
-/. - c.1725G>A r.(?) p.(=)
-/. - c.1755C>T r.(?) p.(Gly585=)
+/. - c.1775G>A r.(?) p.(Arg592Gln)
-?/. - c.1821C>T r.(?) p.(Tyr607=)
?/. - c.1822G>A r.(?) p.(Ala608Thr)
-/. - c.1890C>T r.(?) p.(Val630=)
?/. - c.1916A>T r.(?) p.(Asp639Val)
-?/. - c.1918C>T r.(?) p.(Arg640Trp)
-?/. - c.1919G>A r.(?) p.(Arg640Gln)
-?/. - c.1919G>A r.(?) p.(Arg640Gln)
?/. - c.1925C>T r.(?) p.(Thr642Met)
?/. - c.1945+5G>A r.spl? p.?
./. - c.1945+992C>T - p.(=)
-/. - c.1992G>A r.(?) p.(Pro664=)
-?/. - c.1992G>A r.(?) p.(Pro664=)
?/. - c.1994C>T r.(?) p.(Ser665Leu)
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