Variant #0000576788 (NC_000023.10:g.55054238C>T, NC_000023.10(NM_000032.4):c.-15-1790G>A (ALAS2))
Chromosome |
X |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.55054238C>T |
DNA change (hg38) |
g.55027805C>T |
Published as |
ALAS2(NM_000032.4):c.-15-1790G>A (p.(=)), ALAS2(NM_001037968.3):c.3G>A (p.M1?), ALAS2(NM_001037968.4):c.3G>A (p.M1?) |
ISCN |
- |
DB-ID |
ALAS2_000015 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) |
0.00285 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2022-05-09 15:51:19 +02:00 (CEST) |

Variant on transcripts
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