Variant #0000982362 (NC_000017.10:g.19575123_19575124del, NM_000382.2:c.1297_1298del (ALDH3A2))
| Chromosome |
17 |
| 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.19575123_19575124del |
| DNA change (hg38) |
- |
| Published as |
ALDH3A2(NM_000382.2):c.1297_1298delGA (p.(Glu433ArgfsTer3)), ALDH3A2(NM_000382.3):c.1297_1298delGA (p.E433Rfs*3), ALDH3A2(NM_001031806.1):c.1297_12... |
| ISCN |
- |
| DB-ID |
ALDH3A2_000010 See all 22 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_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2024-04-19 20:27:30 +02:00 (CEST) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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