Variant #0000692288 (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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2020-09-15 15:50:26 +02:00 (CEST) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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