Variant #0000804134 (NC_000009.11:g.36966688G>A, NM_016734.2:c.638C>T (PAX5))

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.36966688G>A
DNA change (hg38) -
Published as PAX5(NM_016734.2):c.638C>T (p.S213L), PAX5(NM_016734.3):c.638C>T (p.S213L)
ISCN -
DB-ID PAX5_000016 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) 0.00061 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PAX5 NM_016734.2 ?/. - c.638C>T r.(?) p.(Ser213Leu)


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