Variant #0000848195 (NC_000004.11:g.187130126C>T, NM_207352.3:c.1198C>T (CYP4V2))
| Chromosome |
4 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.187130126C>T |
| DNA change (hg38) |
g.186208972C>T |
| Published as |
CYP4V2 c.1198C>T, R400C |
| ISCN |
- |
| DB-ID |
CYP4V2_000023 See all 16 reported entries |
| Variant remarks |
homozygous |
| Reference |
PubMed: Lockhart 2018 |
| ClinVar ID |
- |
| dbSNP ID |
- |
| Origin |
Unknown |
| Segregation |
? |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
5.0E-5 View details |
| Owner |
LOVD |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
Anna Tracewska |
| Date created |
2022-05-09 15:31:45 +02:00 (CEST) |
| Date last edited |
2025-03-09 08:49:29 +01:00 (CET) |

Variant on transcripts
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