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 100 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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