Variant #0000924438 (NC_000006.11:g.146007166G>A, NC_000006.11(NM_001018041.1):c.476+92C>T (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.146007166G>A
DNA change (hg38) -
Published as EPM2A(NM_001360071.2):c.62+92C>T
ISCN -
DB-ID EPM2A_000029
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_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.476+92C>T r.(=) p.(=)


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