Variant #0000658331 (NC_000018.9:g.21353577_21353592del, LAMA3(NM_198129.1):c.1273+26_1273+41del)
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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