Variant #0000370400 (NC_000006.11:g.129371234G>C, NC_000006.11(NM_000426.3):c.283+1G>C (LAMA2))
Chromosome |
6 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Affects function |
Classification method |
ACMG |
Clinical classification |
pathogenic (recessive) |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.129371234G>C |
DNA change (hg38) |
g.129050089G>C |
Published as |
- |
ISCN |
- |
DB-ID |
LAMA2_000473 See all 5 reported entries |
Variant remarks |
- |
Reference |
PubMed: Oliveira 2018, Journal: Oliveira 2018 |
ClinVar ID |
- |
dbSNP ID |
- |
Origin |
SUMMARY record |
Segregation |
- |
Frequency |
- |
Re-site |
- |
VIP |
- |
Methylation |
- |
Average frequency (gnomAD v.2.1.1) |
Retrieve |
Owner |
Jorge Oliveira |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
Johan den Dunnen |
Date created |
2018-06-29 15:10:22 +02:00 (CEST) |
Date last edited |
2020-06-19 20:22:21 +02:00 (CEST) |

Variant on transcripts
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