Variant #0000950033 (NC_000012.11:g.7361644C>T, NM_000319.4:c.1414C>T (PEX5))
| Chromosome |
12 |
| 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.7361644C>T |
| DNA change (hg38) |
- |
| Published as |
PEX5(NM_000319.4):c.1414C>T (p.(Arg472Trp)), PEX5(NM_001131025.2):c.1438C>T (p.R480W) |
| ISCN |
- |
| DB-ID |
PEX5_000036 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) |
2.0E-5 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2023-11-27 17:35:39 +01:00 (CET) |
| Date last edited |
N/A |

Variant on transcripts
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