Variant #0000801869 (NC_000005.9:g.128796881A>C, NM_133638.3:c.160A>C (ADAMTS19))
| Chromosome |
5 |
| 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.128796881A>C |
| DNA change (hg38) |
- |
| Published as |
ADAMTS19(NM_133638.4):c.178A>C (p.S60R), ADAMTS19(NM_133638.5):c.178A>C (p.S60R), ADAMTS19(NM_133638.6):c.178A>C (p.(Ser60Arg)) |
| ISCN |
- |
| DB-ID |
ADAMTS19_000009 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) |
0.00074 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
| Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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