Variant #0001062772 (NC_000001.10:g.152084741_152084761dup, NM_007113.3:c.958_978dup (TCHH))

Chromosome 1
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.152084741_152084761dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID TCHH_000022
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
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 2026-01-13 13:39:01 +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     
TCHH NM_007113.3 -?/. - c.958_978dup r.(?) p.(Glu320_Glu326dup)


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