Variant #0000677264 (NC_000004.11:g.2828992C>T, NM_003023.4:c.464C>T (SH3BP2))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.2828992C>T
DNA change (hg38) -
Published as SH3BP2(NM_001122681.1):c.464C>T (p.(Ala155Val)), SH3BP2(NM_001145855.2):c.548C>T (p.A183V)
ISCN -
DB-ID SH3BP2_000010 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) 0.0053 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 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.464C>T r.(?) p.(Ala155Val)


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