Variant #0000522426 (NC_000004.11:g.2824764G>A, NM_003023.4:c.239G>A (SH3BP2))

Chromosome 4
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.2824764G>A
DNA change (hg38) g.2823037G>A
Published as SH3BP2(NM_001122681.2):c.239G>A (p.(Arg80Gln)), SH3BP2(NM_001145855.2):c.323G>A (p.R108Q), SH3BP2(NM_001145856.1):c.410G>A (p.R137Q)
ISCN -
DB-ID SH3BP2_000027 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) 0.00036 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SH3BP2 NM_003023.4 ?/. - c.239G>A r.(?) p.(Arg80Gln)


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