Variant #0000692729 (NC_000019.9:g.19257169G>A, NM_001145783.1:c.*36209C>T (MEF2BNB))

Chromosome 19
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.19257169G>A
DNA change (hg38) -
Published as MEF2B(NM_001145785.2):c.794C>T (p.P265L)
ISCN -
DB-ID MEF2B_000003
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 2020-09-15 15:50:26 +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     
MEF2BNB NM_001145783.1 -?/. - c.*36209C>T r.(=) p.(=)
MEF2B NM_001145785.1 -?/. - c.794C>T r.(?) p.(Pro265Leu)
MEF2BNB-MEF2B NM_005919.3 -?/. - c.769+195C>T r.(=) p.(=)


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