Variant #0000806555 (NC_000015.9:g.100252738_100252743dup, NM_001130926.1:c.1256_1261dup (MEF2A))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100252738_100252743dup
DNA change (hg38) -
Published as MEF2A(NM_001352615.1):c.1256_1261dupAGCAGC (p.Q419_Q420dup)
ISCN -
DB-ID MEF2A_000016
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEF2A NM_001130926.1 -/. - c.1256_1261dup r.(?) p.(Gln419_Gln420dup)


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