Variant #0000338976 (NC_000007.13:g.143013488A>T, NC_000007.13(NM_000083.2):c.180+3A>T (CLCN1))
Chromosome |
7 |
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.143013488A>T |
DNA change (hg38) |
g.143316395A>T |
Published as |
- |
ISCN |
- |
DB-ID |
CLCN1_000005 See all 21 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) |
0.00029 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-23 14:34:09 +02:00 (CEST) |

Variant on transcripts
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