Variant #0001052861 (NC_000007.13:g.139655341C>G, NM_001061.4:c.626C>G (TBXAS1))

Chromosome 7
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.139655341C>G
DNA change (hg38) -
Published as TBXAS1(NM_001061.7):c.623C>G (p.(Pro208Arg)), TBXAS1(NM_001130966.2):c.626C>G (p.P209R)
ISCN -
DB-ID TBXAS1_000006 See all 3 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) 0.00037 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
TBXAS1 NM_001061.4 ?/. - c.626C>G r.(?) p.(Pro209Arg)


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