Variant #0001075642 (NC_000015.9:g.43905434G>T, NC_000015.9(NM_153700.2):c.2481-5C>A (STRC))

Chromosome 15
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.43905434G>T
DNA change (hg38) -
Published as -
ISCN -
DB-ID STRC_000117
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1467789363
Origin Unknown
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 2026-04-28 11:32:01 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
STRC NM_153700.2 ?/. - c.2481-5C>A r.(?) p.(?)


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