Variant #0000658331 (NC_000018.9:g.21353577_21353592del, NC_000018.9(NM_198129.1):c.1273+26_1273+41del (LAMA3))
| 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.21353577_21353592del |
| DNA change (hg38) |
g.23773613_23773628del |
| Published as |
LAMA3(NM_001302996.2):c.1299_1314delTCTTAGCCTGTGTGTA (p.L434Cfs*31) |
| ISCN |
- |
| DB-ID |
LAMA3_000049 |
| 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_Groningen |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Groningen |
| Date created |
2020-03-23 16:13:27 +01:00 (CET) |
| Date last edited |
2021-09-17 14:40:49 +02:00 (CEST) |

Variant on transcripts
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