Variant #0000924439 (NC_000006.11:g.146056681C>T, NM_001018041.1:c.-47G>A (EPM2A))

Chromosome 6
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.146056681C>T
DNA change (hg38) -
Published as EPM2A(NM_001360064.2):c.-114+363G>A
ISCN -
DB-ID EPM2A_000030
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) 0.48947 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPM2A NM_001018041.1 -/. - c.-47G>A r.(?) p.(=)
FBXO30 NM_032145.4 -/. - c.*64561G>A r.(=) p.(=)
SHPRH NM_173082.3 -/. - c.*150883G>A r.(=) p.(=)


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