Variant #0000345035 (NC_000019.9:g.19304811C>G, NM_001145783.1:c.-1885G>C (MEF2BNB))

Chromosome 19
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.19304811C>G
DNA change (hg38) g.19194002C>G
Published as -
ISCN -
DB-ID RFXANK_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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
MEF2BNB NM_001145783.1 +/. - c.-1885G>C r.(?) p.(=)
MEF2B NM_001145785.1 +/. - c.-23827G>C r.(?) p.(=)
RFXANK NM_003721.2 +/. - c.56C>G r.(?) p.(Ser19Ter)
MEF2BNB-MEF2B NM_005919.3 +/. - c.-2138G>C r.(?) p.(=)
NR2C2AP NM_176880.4 +/. - c.*7923G>C r.(=) p.(=)


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