Variant #0000520886 (NC_000003.11:g.9985169G>A, NM_015513.4:c.1018G>A (CRELD1))
Chromosome |
3 |
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.9985169G>A |
DNA change (hg38) |
g.9943485G>A |
Published as |
CRELD1(NM_001077415.3):c.1018G>A (p.(Glu340Lys)), CRELD1(NM_015513.6):c.1018G>A (p.E340K) |
ISCN |
- |
DB-ID |
CRELD1_000014 See all 2 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_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|