Variant #0000912672 (NC_000007.13:g.139611050T>C, NM_001061.4:c.266T>C (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.139611050T>C
DNA change (hg38) -
Published as TBXAS1(NM_001061.4):c.266T>C (p.(Ile89Thr)), TBXAS1(NM_001130966.2):c.266T>C (p.I89T)
ISCN -
DB-ID TBXAS1_000026 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) 0.00033 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 2023-01-11 15:44:22 +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.266T>C r.(?) p.(Ile89Thr)


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