Variant #0001046879 (NC_000023.10:g.70073098G>A, NM_001003811.1:c.450C>T (TEX11))

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.70073098G>A
DNA change (hg38) -
Published as TEX11(NM_001003811.1):c.450C>T (p.(=)), TEX11(NM_001003811.2):c.450C>T (p.A150=)
ISCN -
DB-ID TEX11_000004 See all 2 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00193 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TEX11 NM_001003811.1 -?/. - c.450C>T r.(?) p.(Ala150=)
TEX11 NM_031276.2 -?/. - c.405C>T r.(?) p.(Ala135=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.