Variant #0000271075 (NC_000023.10:g.69176943C>T, NM_001399.4:c.463C>T (EDA))

Chromosome X
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.69176943C>T
DNA change (hg38) g.69957093C>T
Published as EDA(NM_001399.4):c.463C>T (p.(Arg155Cys)), EDA(NM_001399.5):c.463C>T (p.R155C)
ISCN -
DB-ID EDA_000069 See all 18 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) Retrieve
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 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EDA NM_001399.4 +/. - c.463C>T r.(?) p.(Arg155Cys)


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