Variant #0000917029 (NC_000003.11:g.150690352A>C, NM_174878.2:c.144T>G (CLRN1))
| Chromosome |
3 |
| Allele |
Unknown |
| Affects function (as reported) |
Probably affects function |
| Affects function (by curator) |
Probably affects function |
| Classification method |
ACMG |
| Clinical classification |
likely pathogenic |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.150690352A>C |
| DNA change (hg38) |
g.150972565A>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
CLRN1_000007 See all 101 reported entries |
| Variant remarks |
PS3_M, PM3_VS |
| Reference |
- |
| ClinVar ID |
- |
| dbSNP ID |
rs111033258 |
| Origin |
SUMMARY record |
| Segregation |
- |
| Frequency |
- |
| Re-site |
- |
| VIP |
- |
| Methylation |
- |
| Average frequency (gnomAD v.2.1.1) |
0.00026 View details |
| Owner |
David Baux |
| Database submission license |
Creative Commons Attribution 4.0 International |
| Created by |
David Baux |
| Date created |
2023-01-17 17:47:01 +01:00 (CET) |
| Date last edited |
2023-01-17 17:48:45 +01:00 (CET) |

Variant on transcripts
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