Variant #0000721978 (NC_000008.10:g.38871509G>A, NM_003816.2:c.280G>A (ADAM9))
Chromosome |
8 |
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.38871509G>A |
DNA change (hg38) |
- |
Published as |
ADAM9(NM_003816.2):c.280G>A (p.V94I, p.(Val94Ile)), ADAM9(NM_003816.3):c.280G>A (p.V94I) |
ISCN |
- |
DB-ID |
ADAM9_000002 See all 5 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) |
0.0021 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2021-02-08 18:36:18 +01:00 (CET) |
Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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