Variant #0000967622 (NC_000015.9:g.100252738_100252743del, NM_001130926.1:c.1256_1261del (MEF2A))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.100252738_100252743del
DNA change (hg38) -
Published as MEF2A(NM_001171894.5):c.1256_1261delAGCAGC (p.Q419_Q420del), MEF2A(NM_001352615.4):c.1256_1261delAGCAGC (p.Q419_Q420del)
ISCN -
DB-ID MEF2A_000002
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2024-02-26 20:06:56 +01:00 (CET)
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_1261del r.(?) p.(Gln419_Gln420del)


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