Variant #0000924700 (NC_000007.13:g.24738646C>G, NM_001127453.1:c.1490G>C (DFNA5))

Chromosome 7
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.24738646C>G
DNA change (hg38) -
Published as -
ISCN -
DB-ID DFNA5_000051
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) 2.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
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     
DFNA5 NM_001127453.1 ?/. - c.1490G>C r.(?) p.(*497Serext*4)
DFNA5 NM_004403.2 ?/. - c.1490G>C r.(?) p.(*497Serext*4)


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