Transcript #00024148 (NM_014000.2, VCL gene)

Transcript name transcript variant 1
Gene name VCL (vinculin)
Chromosome 10
Transcript - NCBI ID NM_014000.2
Transcript - Ensembl ID -
Protein - NCBI ID NP_054706.1
Protein - Ensembl ID -
Protein - Uniprot ID -
Exon/intron information Exon/intron information table: HTML, Txt
Remarks -
Date created 2016-06-18 18:42:56 +02:00 (CEST)
Date last edited N/A


Variants

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

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     
?/. - c.4C>G r.(?) p.(Pro2Ala)
?/. - c.20G>T r.(?) p.(Arg7Leu)
-?/. - c.30G>A r.(?) p.(Glu10=)
-?/. - c.36C>T r.(?) p.(Ile12=)
-?/. - c.36C>T r.(?) p.(Ile12=)
?/. - c.78G>A r.(?) p.(Met26Ile)
-/. - c.81C>T r.(?) p.(His27=)
-?/. - c.81C>T r.(?) p.(His27=)
-?/. - c.81C>T r.(?) p.(His27=)
-?/. - c.81C>T r.(?) p.(His27=)
?/. - c.98A>G r.(?) p.(Asp33Gly)
-/. - c.108C>T r.(?) p.(Ala36=)
-/. - c.120C>T r.(?) p.(Leu40=)
-?/. - c.120C>T r.(?) p.(Leu40=)
?/. - c.122C>T r.(?) p.(Thr41Ile)
?/. - c.151G>A r.(?) p.(Val51Ile)
?/. - c.152T>G r.(?) p.(Val51Gly)
?/. - c.167G>A r.(?) p.(Arg56Gln)
?/. - c.167G>C r.(?) p.(Arg56Pro)
-?/. - c.168G>C r.(?) p.(Arg56=)
?/. - c.168+1G>A r.spl? p.?
-?/. - c.168+9G>T r.(=) p.(=)
-/. - c.168+9G>T r.(=) p.(=)
-?/. - c.168+14G>T r.(=) p.(=)
-/. - c.168+18G>A r.(=) p.(=)
?/. - c.168+20C>T r.(=) p.(=)
-?/. - c.169-20G>T r.(=) p.(=)
-/. - c.169-11dup r.(=) p.(=)
-/. - c.169-11T>C r.(=) p.(=)
-?/. - c.169-10C>G r.(=) p.(=)
-/. - c.169-10C>G r.(=) p.(=)
?/. - c.184G>A r.(?) p.(Val62Ile)
?/. - c.184_185del r.(?) p.(Val62SerfsTer4)
-?/. - c.189A>G r.(?) p.(Gln63=)
?/. - c.224C>T r.(?) p.(Pro75Leu)
-?/. - c.239+6T>G r.(=) p.(=)
?/. - c.239+6T>G r.(=) p.(=)
-?/. - c.239+11G>A r.(=) p.(=)
-?/. - c.252T>A r.(?) p.(Ala84=)
-?/. - c.252T>A r.(?) p.(Ala84=)
+?/. - c.286C>T r.(?) p.(Gln96Ter)
+?/. - c.313C>T r.(?) p.(Arg105*)
-/. - c.339G>A r.(?) p.(Arg113=)
-?/. - c.339G>A r.(?) p.(Arg113=)
-/. - c.339G>A r.(?) p.(Arg113=)
-?/. - c.345C>T r.(?) p.(Ile115=)
-?/. - c.366G>A r.(?) p.(Leu122=)
-?/. - c.366G>A r.(?) p.(Leu122=)
-/. - c.366G>A r.(?) p.(Leu122=)
-?/. - c.378C>T r.(?) p.(Phe126=)
-/. - c.378C>T r.(?) p.(Phe126=)
?/. - c.379G>A r.(?) p.(Asp127Asn)
?/. - c.379G>A r.(?) p.(Asp127Asn)
?/. - c.379G>A r.(?) p.(Asp127Asn)
-/. - c.384G>A r.(?) p.(Glu128=)
?/. - c.391G>A r.(?) p.(Val131Ile)
?/. - c.391G>A r.(?) p.(Val131Ile)
-?/. - c.404T>C r.(?) p.(Ile135Thr)
-/. - c.404T>C r.(?) p.(Ile135Thr)
-/. - c.406A>C r.(?) p.(Arg136=)
-?/. - c.424T>C r.(?) p.(Leu142=)
-/. - c.424T>C r.(?) p.(Leu142=)
?/. - c.445G>A r.(?) p.(Glu149Lys)
-?/. - c.492T>G r.(?) p.(Leu164=)
-?/. - c.492T>G r.(?) p.(Leu164=)
-?/. - c.492T>G r.(?) p.(Leu164=)
-?/. - c.492T>G r.(?) p.(Leu164=)
-/. - c.492T>G r.(?) p.(Leu164=)
?/. - c.494G>A r.(?) p.(Gly165Glu)
-?/. - c.499+19C>T r.(=) p.(=)
?/. - c.518A>G r.(?) p.(Lys173Arg)
-?/. - c.528C>T r.(?) p.(Asp176=)
-?/. - c.528C>T r.(?) p.(Asp176=)
-/. - c.528C>T r.(?) p.(Asp176=)
-/. - c.531G>A r.(?) p.(Glu177=)
?/. - c.539A>G r.(?) p.(Gln180Arg)
?/. - c.539A>G r.(?) p.(Gln180Arg)
?/. - c.539A>G r.(?) p.(Gln180Arg)
+?/. - c.562C>T r.(?) p.(Arg188*)
-?/. - c.565G>A r.(?) p.(Val189Met)
?/. - c.565G>A r.(?) p.(Val189Met)
?/. - c.590C>T r.(?) p.(Thr197Ile)
-?/. - c.590C>T r.(?) p.(Thr197Ile)
-?/. - c.590C>T r.(?) p.(Thr197Ile)
?/. - c.592G>A r.(?) p.(Val198Met)
?/. - c.592G>A r.(?) p.(Val198Met)
-/. - c.606G>A r.(?) p.(Leu202=)
?/. - c.610G>C r.(?) p.(Val204Leu)
-?/. - c.622+4C>G r.spl? p.?
-?/. - c.622+4C>G r.spl? p.?
-?/. - c.622+4C>G r.spl? p.?
-/. - c.622+4C>G r.spl? p.?
-?/. - c.622+4C>T r.spl? p.?
-?/. - c.622+4C>T r.spl? p.?
-/. - c.622+4C>T r.spl? p.?
-/. - c.623-30A>G r.(=) p.(=)
-/. - c.623-30A>G r.(=) p.(=)
-?/. - c.650A>G r.(?) p.(Asn217Ser)
+?/. - c.659dup r.(?) p.(Asn220Lysfs*21)
-?/. - c.660C>T r.(?) p.(Asn220=)
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