Variant #0000369944 (NC_000006.11:g.129204392T>C, NM_000426.3:c.2T>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.129204392T>C |
| DNA change (hg38) |
g.128883247T>C |
| Published as |
- |
| ISCN |
- |
| DB-ID |
LAMA2_000003 See all 6 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 |
2019-02-28 09:09:39 +01:00 (CET) |

Variant on transcripts
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