Variant #0000655138 (NC_000004.11:g.2824764G>A, NM_003023.4:c.239G>A (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.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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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