Variant #0000809788 (NC_000023.10:g.110463619A>G, NM_002578.3:c.1579A>G (PAK3))
Chromosome |
X |
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.110463619A>G |
DNA change (hg38) |
- |
Published as |
PAK3(NM_001128168.2):c.1687A>G (p.S563G), PAK3(NM_001128168.3):c.1687A>G (p.S563G), PAK3(NM_002578.5):c.1579A>G (p.S527G) |
ISCN |
- |
DB-ID |
PAK3_000066 See all 5 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) |
0.00014 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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