Variant #0001037024 (NC_000008.10:g.6357416C>T, NM_001118887.1:c.*3206G>A (ANGPT2))
Chromosome |
8 |
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.6357416C>T |
DNA change (hg38) |
- |
Published as |
MCPH1(NM_024596.4):c.2180C>T (p.P727L), MCPH1(NM_024596.5):c.2180C>T (p.(Pro727Leu), p.P727L) |
ISCN |
- |
DB-ID |
ANGPT2_000018 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) |
0.00098 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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