Variant #0000851580 (NC_000007.13:g.2583390dup, NM_152743.3:c.638dup (BRAT1))
| Chromosome |
7 |
| Allele |
Unknown |
| Affects function (as reported) |
Affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2583390dup |
| DNA change (hg38) |
- |
| Published as |
BRAT1(NM_001350626.1):c.638dupA (p.V214Gfs*189), BRAT1(NM_152743.4):c.638dup (p.(Val214GlyfsTer189)), BRAT1(NM_152743.4):c.638dupA (p.V214Gfs*189) |
| ISCN |
- |
| DB-ID |
BRAT1_000010 See all 11 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) |
Retrieve |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
| Date last edited |
2025-11-01 13:22:20 +01:00 (CET) |

Variant on transcripts
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