Variant #0000566544 (NC_000019.9:g.17397497_17397500del, NM_152363.5:c.*136_*139del (ANKLE1))
Chromosome |
19 |
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.17397497_17397500del |
DNA change (hg38) |
g.17286688_17286691del |
Published as |
ANKLE1(NM_001278443.1):c.*96_*99del (p.(=)), ANKLE1(NM_001278444.2):c.1767_1770delGTGT (p.L591Vfs*17) |
ISCN |
- |
DB-ID |
ANKLE1_000007 See all 2 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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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