Variant #0000974844 (NC_000002.11:g.197183858C>T, NM_020760.1:c.1756G>A (HECW2))
Chromosome |
2 |
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.197183858C>T |
DNA change (hg38) |
- |
Published as |
HECW2(NM_020760.4):c.1756G>A (p.D586N) |
ISCN |
- |
DB-ID |
HECW2_000062 |
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) |
7.0E-5 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2024-04-19 20:20:39 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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