Transcript #00014161 (NM_053025.3, MYLK gene)

Transcript name transcript variant 1
Gene name MYLK (myosin light chain kinase)
Chromosome 3
Transcript - NCBI ID NM_053025.3
Transcript - Ensembl ID -
Protein - NCBI ID NP_444253.3
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

473 entries on 5 pages. Showing entries 1 - 100.
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Affects function     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
-?/. - c.-186+11C>G r.(=) p.(=)
-/. - c.-153C>T r.(?) p.(=)
?/. - c.-3A>G r.(?) p.(=)
-?/. - c.24C>G r.(?) p.(Ala8=)
-/. - c.62C>A r.(?) p.(Pro21His)
-/. - c.62C>A r.(?) p.(Pro21His)
?/. - c.119G>A r.(?) p.(Arg40Gln)
?/. - c.139G>A r.(?) p.(Gly47Arg)
-?/. - c.166-160A>T r.(=) p.(=)
?/. - c.169C>T r.(?) p.(Arg57Trp)
-?/. - c.174T>C r.(?) p.(Gly58=)
-?/. - c.207C>T r.(?) p.(Asn69=)
-?/. - c.207C>T r.(?) p.(Asn69=)
-?/. - c.256C>T r.(?) p.(Arg86Trp)
?/. - c.256C>T r.(?) p.(Arg86Trp)
?/. - c.256C>T r.(?) p.(Arg86Trp)
?/. - c.256C>T r.(?) p.(Arg86Trp)
-?/. - c.260G>A r.(?) p.(Gly87Glu)
?/. - c.304G>C r.(?) p.(Gly102Arg)
?/. - c.304G>C r.(?) p.(Gly102Arg)
?/. - c.304G>C r.(?) p.(Gly102Arg)
-?/. - c.312T>C r.(?) p.(Tyr104=)
?/. - c.330T>A r.(?) p.(Asn110Lys)
?/. - c.344G>A r.(?) p.(Arg115His)
?/. 5 c.344G>A r.(?) p.(Arg115His)
-?/. - c.373+18C>G r.(=) p.(=)
-/. - c.373+18C>T r.(=) p.(=)
-/. - c.373+18C>T r.(=) p.(=)
-?/. - c.374-189A>G r.(=) p.(=)
-?/. - c.376A>C r.(?) p.(Ser126Arg)
-?/. - c.382G>A r.(?) p.(Ala128Thr)
-?/. - c.382G>A r.(?) p.(Ala128Thr)
-?/. - c.383C>T r.(?) p.(Ala128Val)
-?/. - c.384G>A r.(?) p.(Ala128=)
-?/. - c.399G>T r.(?) p.(Gln133His)
-?/. - c.399G>T r.(?) p.(Gln133His)
-?/. - c.399G>T r.(?) p.(Gln133His)
-/. - c.411C>G r.(?) p.(Ser137=)
-/. - c.411C>G r.(?) p.(Ser137=)
-/. - c.422+14G>C r.(=) p.(=)
-?/. - c.422+168G>C r.(=) p.(=)
?/. - c.424G>T r.(?) p.(Asp142Tyr)
-/. - c.439C>T r.(?) p.(Pro147Ser)
-/. - c.439C>T r.(?) p.(Pro147Ser)
-/. - c.439C>T r.(?) p.(Pro147Ser)
+?/. 8 c.439C>T r.(439C>T) p.(Pro147Ser)
-?/. - c.443C>T r.(?) p.(Ala148Val)
-?/. - c.454C>T r.(?) p.(Arg152Cys)
-?/. - c.455G>A r.(?) p.(Arg152His)
-?/. - c.455G>A r.(?) p.(Arg152His)
?/. - c.463A>G r.(?) p.(Ile155Val)
?/. - c.463A>G r.(?) p.(Ile155Val)
-?/. - c.465C>A r.(?) p.(Ile155=)
-/. - c.479C>G r.(?) p.(Pro160Arg)
-/. - c.479C>G r.(?) p.(Pro160Arg)
-/. - c.479C>G r.(?) p.(Pro160Arg)
?/. - c.493del r.(?) p.(Thr165ProfsTer72)
?/. - c.493del r.(?) p.(Thr165ProfsTer72)
?/. - c.493del r.(?) p.(Thr165ProfsTer72)
?/. - c.506G>A r.(?) p.(Arg169Gln)
?/. - c.575T>C r.(?) p.(Val192Ala)
?/. - c.575T>C r.(?) p.(Val192Ala)
-/. - c.588+13_588+16del r.(=) p.(=)
-?/. - c.588+13_588+16del r.(=) p.(=)
-?/. - c.588+17C>T r.(=) p.(=)
-/. - c.589-30A>T r.(=) p.(=)
-?/. - c.609G>C r.(?) p.(Pro203=)
-/. - c.652C>T r.(?) p.(Leu218=)
-/. - c.652C>T r.(?) p.(Leu218=)
-/. - c.652C>T r.(?) p.(Leu218=)
-?/. - c.681C>T r.(?) p.(=)
-?/. - c.682G>C r.(?) p.(Val228Leu)
-?/. - c.684G>T r.(?) p.(Val228=)
?/. - c.697T>G r.(?) p.(Cys233Gly)
-?/. - c.711C>T r.(?) p.(Asn237=)
-?/. - c.711C>T r.(?) p.(Asn237=)
-?/. - c.717G>A r.(?) p.(Ser239=)
?/. - c.717G>A r.(?) p.(Ser239=)
?/. - c.745T>G r.(?) p.(Ser249Ala)
?/. - c.754+1G>A r.spl? p.?
-?/. - c.754+16C>T r.(=) p.(=)
-?/. - c.754+17G>A r.(=) p.(=)
-/. - c.755-12C>T r.(=) p.(=)
-?/. - c.755-12C>T r.(=) p.(=)
-/. - c.755-12C>T r.(=) p.(=)
-?/. - c.773+67A>T r.(=) p.(=)
-?/. - c.774-18A>C r.(=) p.(=)
-?/. - c.774-15C>G r.(=) p.(=)
-?/. - c.774-15C>G r.(=) p.(=)
-?/. - c.774-10C>T r.(=) p.(=)
-/. - c.782T>C r.(?) p.(Val261Ala)
-/. - c.782T>C r.(?) p.(Val261Ala)
-/. - c.782T>C r.(?) p.(Val261Ala)
+/. - c.937C>T r.(?) p.(Gln313Ter)
-?/. - c.984G>A r.(?) p.(Ser328=)
-?/. - c.993G>A r.(?) p.(Thr331=)
-?/. - c.999G>A r.(?) p.(Pro333=)
-?/. - c.999G>A r.(?) p.(Pro333=)
-?/. - c.999G>A r.(?) p.(Pro333=)
-?/. - c.999G>A r.(?) p.(Pro333=)
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