Variant #0000678840 (NC_000010.10:g.28224092C>A, NM_018076.2:c.2342G>T (ARMC4))
| Chromosome |
10 |
| 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.28224092C>A |
| DNA change (hg38) |
- |
| Published as |
ARMC4(NM_001290020.1):c.2342G>T (p.G781V), ARMC4(NM_018076.2):c.2342G>T (p.(Gly781Val)), ODAD2(NM_018076.5):c.2342G>T (p.G781V) |
| ISCN |
- |
| DB-ID |
ARMC4_000019 See all 4 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) |
0.00203 View details |
| Owner |
VKGL-NL_Rotterdam |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Rotterdam |
| Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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