Variant #0000559184 (NC_000016.9:g.77353802T>G, NM_199355.2:c.2476A>C (ADAMTS18))
| Chromosome |
16 |
| 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.77353802T>G |
| DNA change (hg38) |
g.77319905T>G |
| Published as |
ADAMTS18(NM_199355.2):c.2476A>C (p.(Asn826His)), ADAMTS18(NM_199355.3):c.2476A>C (p.N826H), ADAMTS18(NM_199355.4):c.2476A>C (p.N826H) |
| ISCN |
- |
| DB-ID |
ADAMTS18_000063 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) |
0.00454 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 |
2023-01-11 15:44:22 +01:00 (CET) |

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