Variant #0001072415 (NC_000023.10:g.122753285G>C, NM_001081550.1:c.4278C>G (THOC2))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.122753285G>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID THOC2_000055
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs751850871
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 2.0E-5 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-04-10 15:53:01 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
THOC2 NM_001081550.1 -?/. - c.4278C>G r.(?) p.(Asp1426Glu)


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