Variant #0000274965 (NC_000007.13:g.24738788G>A, NM_001127453.1:c.1348C>T (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.24738788G>A
DNA change (hg38) g.24699169G>A
Published as DFNA5(NM_004403.2):c.1348C>T (p.R450C)
ISCN -
DB-ID DFNA5_000002
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) 0.001 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNA5 NM_001127453.1 ?/. - c.1348C>T r.(?) p.(Arg450Cys)
DFNA5 NM_004403.2 ?/. - c.1348C>T r.(?) p.(Arg450Cys)


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