Variant #0001053277 (NC_000009.11:g.88203292G>A, NM_015239.2:c.2704C>T (AGTPBP1))

Chromosome 9
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.88203292G>A
DNA change (hg38) -
Published as AGTPBP1(NM_001286715.1):c.2980C>T (p.P994S), AGTPBP1(NM_001330701.2):c.2824C>T (p.(Pro942Ser))
ISCN -
DB-ID AGTPBP1_000001 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) 0.00011 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
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
AGTPBP1 NM_015239.2 ?/. - c.2704C>T r.(?) p.(Pro902Ser)


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