Variant #0000301446 (NC_000019.9:g.19304899G>C, NM_001145783.1:c.-1973C>G (MEF2BNB))

Chromosome 19
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.19304899G>C
DNA change (hg38) g.19194090G>C
Published as RFXANK(NM_003721.2):c.144G>C (p.E48D)
ISCN -
DB-ID RFXANK_000001 See all 2 reported entries
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) 0.05313 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 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.-1973C>G r.(?) p.(=)
MEF2B NM_001145785.1 -/. - c.-23915C>G r.(?) p.(=)
RFXANK NM_003721.2 -/. - c.144G>C r.(?) p.(Glu48Asp)
MEF2BNB-MEF2B NM_005919.3 -/. - c.-2226C>G r.(?) p.(=)
NR2C2AP NM_176880.4 -/. - c.*7835C>G r.(=) p.(=)


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