Variant #0000273908 (NC_000021.8:g.46930005_46930006del, NM_030582.3:c.4054_4055del (COL18A1))
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.46930005_46930006del |
DNA change (hg38) |
g.45510091_45510092del |
Published as |
COL18A1(NM_001379500.1):c.3523_3524del (p.(Leu1175fs)), COL18A1(NM_001379500.1):c.3523_3524delCT (p.L1175Vfs*72), COL18A1(NM_130445.2):c.3514_3515d... |
ISCN |
- |
DB-ID |
COL18A1_000002 See all 12 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) |
0.0003 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|