Variant #0000604217 (NC_000001.10:g.94486791C>T, NC_000001.10(NM_000350.2):c.5018+5G>A (ABCA4))
Chromosome |
1 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
NA |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.94486791C>T |
DNA change (hg38) |
g.94021235C>T |
Published as |
- |
ISCN |
- |
DB-ID |
ABCA4_001253 See all 17 reported entries |
Variant remarks |
- |
Reference |
PubMed: Fadaie et al 2019; Journal: Fadaie et al 2019 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Zeinab Fadaie |
Database submission license |
Creative Commons Attribution-ShareAlike 4.0 International |
Created by |
Ivo F.A.C. Fokkema |
Date created |
2019-11-18 12:54:55 +01:00 (CET) |
Date last edited |
2020-07-14 21:57:48 +02:00 (CEST) |

Variant on transcripts
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