Variant #0000515777 (NC_000002.11:g.38298290_38298299dup, NM_000104.3:c.1200_1209dup (CYP1B1))
Chromosome |
2 |
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.38298290_38298299dup |
DNA change (hg38) |
g.38071147_38071156dup |
Published as |
CYP1B1(NM_000104.3):c.1209_1210insTCATGCCACC (p.H403_H404=) |
ISCN |
- |
DB-ID |
CYP1B1_000022 See all 15 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 |
2020-08-06 14:59:34 +02:00 (CEST) |

Variant on transcripts
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