Variant #0001035417 (NC_000006.11:g.112575014A>G, NC_000006.11(NM_001105206.2):c.195+144T>C (LAMA4))
| Chromosome |
6 |
| Allele |
Unknown |
| Affects function (as reported) |
Does not affect function |
| Affects function (by curator) |
Not classified |
| Classification method |
- |
| Clinical classification |
benign |
| DNA change (genomic) (Relative to hg19 / GRCh37) |
g.112575014A>G |
| DNA change (hg38) |
- |
| Published as |
LAMA4(NM_001105208.1):c.339T>C (p.L113=), LAMA4(NM_001105208.3):c.339T>C (p.(Leu113=)), LAMA4(NM_001105209.3):c.339T>C (p.L113=) |
| ISCN |
- |
| DB-ID |
LAMA4_000132 See all 4 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) |
0.01378 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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