Variant #0000148367 (NC_000008.10:g.41571774T>G, NC_000008.10(NM_000037.3):c.1702-2A>C (ANK1))
Chromosome |
8 |
Allele |
Unknown |
Affects function (as reported) |
Probably affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.41571774T>G |
DNA change (hg38) |
g.41714256T>G |
Published as |
- |
ISCN |
- |
DB-ID |
ANK1_000013 |
Variant remarks |
- |
Reference |
- |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
Unknown |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
MANSOUR-HENDILI |
Database submission license |
No license selected |
Created by |
MANSOUR-HENDILI |
Date created |
2016-12-08 13:53:38 +01:00 (CET) |
Date last edited |
2024-03-06 10:04:46 +01:00 (CET) |

Variant on transcripts
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