Variant #0001017944 (NC_000007.13:g.24742436_24742437inv, NM_001127453.1:c.1199_1200inv (DFNA5))

Chromosome 7
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.24742436_24742437inv
DNA change (hg38) -
Published as -
ISCN -
DB-ID DFNA5_000052
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2024-12-06 11:30:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DFNA5 NM_001127453.1 -/. - c.1199_1200inv r.(?) p.(Ala400Val)


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