Variant #0001042521 (NC_000018.9:g.7050910A>G, NM_005559.3:c.371T>C (LAMA1))
| Chromosome |
18 |
| Allele |
Unknown |
| Affects function (as reported) |
Effect unknown |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
VUS |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.7050910A>G |
| DNA change (hg38) |
- |
| Published as |
LAMA1(NM_005559.3):c.371T>C (p.I124T), LAMA1(NM_005559.4):c.371T>C (p.(Ile124Thr), p.I124T) |
| ISCN |
- |
| DB-ID |
LAMA1_000209 See all 3 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) |
0.00015 View details |
| Owner |
VKGL-NL_Leiden |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Leiden |
| Date created |
2025-05-05 21:14:00 +02:00 (CEST) |
| Date last edited |
N/A |

Variant on transcripts
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