Variant #0000849720 (NC_000002.11:g.219674320C>T, NM_000784.3:c.276C>T (CYP27A1))
| Chromosome |
2 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.219674320C>T |
| DNA change (hg38) |
- |
| Published as |
CYP27A1(NM_000784.3):c.276C>T (p.Y92=), CYP27A1(NM_000784.4):c.276C>T (p.Y92=) |
| ISCN |
- |
| DB-ID |
CYP27A1_000107 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) |
0.00037 View details |
| Owner |
VKGL-NL_Nijmegen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Nijmegen |
| Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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