Variant #0000526908 (NC_000006.11:g.112575087_112575089del, NC_000006.11(NM_001105206.2):c.195+71_195+73del (LAMA4))
| Chromosome |
6 |
| 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.112575087_112575089del |
| DNA change (hg38) |
g.112253885_112253887del |
| Published as |
LAMA4(NM_001105209.2):c.266_268delTCT (p.F89del), LAMA4(NM_001105209.3):c.266_268delTCT (p.F89del) |
| ISCN |
- |
| DB-ID |
LAMA4_000271 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) |
Retrieve |
| Owner |
VKGL-NL_AMC |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_AMC |
| Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
| Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

Variant on transcripts
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