Variant #0000860725 (NC_000007.13:g.24747874C>T, NC_000007.13(NM_001127453.1):c.863-1G>A (DFNA5))

Chromosome 7
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.24747874C>T
DNA change (hg38) -
Published as GSDME(NM_004403.2):c.863-1G>A
ISCN -
DB-ID DFNA5_000048
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNA5 NM_001127453.1 +/. - c.863-1G>A r.spl? p.?
DFNA5 NM_004403.2 +/. - c.863-1G>A r.spl? p.?


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