Variant #0001080435 (NC_000023.10:g.122757903T>C, NC_000023.10(NM_001081550.1):c.3318+8A>G (THOC2))

Chromosome X
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.122757903T>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID chrX_020492
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs909269528
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 2026-07-22 15:52:02 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THOC2 NM_001081550.1 ?/. - c.3318+8A>G r.(?) p.(?)


Screenscraping/webscraping (interacting with LOVD using scripts to download data) is strictly prohibited.
Use our APIs to retrieve data.