Variant #0000543517 (NC_000011.9:g.22257752G>T, NM_213599.2:c.692G>T (ANO5))
Chromosome |
11 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.22257752G>T |
DNA change (hg38) |
g.22236206G>T |
Published as |
ANO5(NM_001142649.1):c.689G>T (p.(Gly230Val)), ANO5(NM_213599.2):c.692G>T (p.G231V), ANO5(NM_213599.3):c.692G>T (p.G231V) |
ISCN |
- |
DB-ID |
ANO5_000005 See all 49 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) |
0.00096 View details |
Owner |
VKGL-NL_VUmc |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_VUmc |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

Variant on transcripts
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