Variant #0000855494 (NC_000019.9:g.19308064C>T, NM_001145783.1:c.-5138G>A (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.19308064C>T
DNA change (hg38) -
Published as RFXANK(NM_003721.2):c.337+4C>T
ISCN -
DB-ID MEF2B_000004
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) 0.0041 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:47:41 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEF2BNB NM_001145783.1 -?/. - c.-5138G>A r.(?) p.(=)
MEF2B NM_001145785.1 -?/. - c.-27080G>A r.(?) p.(=)
RFXANK NM_003721.2 -?/. - c.337+4C>T r.spl? p.?
MEF2BNB-MEF2B NM_005919.3 -?/. - c.-5391G>A r.(?) p.(=)
NR2C2AP NM_176880.4 -?/. - c.*4670G>A r.(=) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.