Variant #0000888469 (NC_000008.10:g.90983460G>A, NM_002485.4:c.643C>T (NBN))
| 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.90983460G>A |
| DNA change (hg38) |
- |
| Published as |
NBN(NM_001024688.2):c.397C>T (p.R133W), NBN(NM_002485.4):c.643C>T (p.R215W, p.(Arg215Trp)), NBN(NM_002485.5):c.643C>T (p.R215W) |
| ISCN |
- |
| DB-ID |
NBN_000020 See all 8 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) |
0.00247 View details |
| Owner |
VKGL-NL_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2022-11-01 13:01:21 +01:00 (CET) |
| Date last edited |
2025-02-07 18:57:27 +01:00 (CET) |

Variant on transcripts
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