Variant #0000852266 (NC_000009.11:g.35095169T>C, NM_032634.3:c.394A>G (PIGO))
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.35095169T>C |
DNA change (hg38) |
- |
Published as |
PIGO(NM_001201484.1):c.394A>G (p.(Met132Val)), PIGO(NM_032634.3):c.394A>G (p.M132V), PIGO(NM_032634.4):c.394A>G (p.M132V) |
ISCN |
- |
DB-ID |
PIGO_000038 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) |
6.0E-5 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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