Variant #0000861696 (NC_000009.11:g.36846910C>T, NM_016734.2:c.1029G>A (PAX5))

Chromosome 9
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.36846910C>T
DNA change (hg38) -
Published as PAX5(NM_001280547.1):c.927G>A (p.(Gly309=)), PAX5(NM_016734.3):c.1029G>A (p.G343=)
ISCN -
DB-ID PAX5_000029 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) 0.02422 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 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2023-04-16 21:50:28 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAX5 NM_016734.2 -/. - c.1029G>A r.(?) p.(Gly343=)


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