Variant #0000975079 (NC_000002.11:g.232123768T>C, NM_025139.4:c.979T>C (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.232123768T>C |
DNA change (hg38) |
- |
Published as |
ARMC9(NM_001352754.2):c.979T>C (p.(Leu327Leu)), ARMC9(NM_025139.6):c.979T>C (p.L327=) |
ISCN |
- |
DB-ID |
ARMC9_000045 See all 2 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) |
0.00039 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2024-04-19 20:20:39 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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