Variant #0000885013 (NC_000002.11:g.232141451G>A, NM_025139.4:c.1437G>A (ARMC9))
Chromosome |
2 |
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.232141451G>A |
DNA change (hg38) |
- |
Published as |
ARMC9(NM_025139.6):c.1437G>A (p.S479=) |
ISCN |
- |
DB-ID |
ARMC9_000043 |
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) |
0.0001 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
2024-08-28 13:07:21 +02:00 (CEST) |

Variant on transcripts
|