Variant #0000405618 (NC_000001.10:g.94495002T>C, NM_000350.2:c.4538A>G (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.94495002T>C |
DNA change (hg38) |
g.94029446T>C |
Published as |
- |
ISCN |
- |
DB-ID |
ABCA4_000533 See all 19 reported entries |
Variant remarks |
expression cloning midigene splicing construct: no correctly spliced RNA |
Reference |
PubMed: Sangermano 2018 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
In vitro (cloned) |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Frans Cremers |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-06-03 10:15:41 +02:00 (CEST) |
Date last edited |
2020-07-14 21:50:58 +02:00 (CEST) |

Variant on transcripts
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