Variant #0001036764 (NC_000008.10:g.143957183G>A, NM_000497.3:c.1066C>T (CYP11B1))
Chromosome |
8 |
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.143957183G>A |
DNA change (hg38) |
- |
Published as |
CYP11B1(NM_000497.3):c.1066C>T (p.Q356*), CYP11B1(NM_000497.4):c.1066C>T (p.(Gln356*), p.Q356*) |
ISCN |
- |
DB-ID |
CYP11B1_000039 See all 4 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) |
6.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
Date last edited |
2025-07-08 13:22:38 +02:00 (CEST) |

Variant on transcripts
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