Variant #0000000632 (NC_000018.9:g.2929099A>G, NM_014646.2:c.1514T>C (LPIN2))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Effect unknown |
Affects function (by curator) |
Effect unknown |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2929099A>G |
Reference |
- |
DB-ID |
LPIN2_000005 |
Frequency |
- |
Average frequency (gnomAD v.2.1.1) |
0.00017 View details |
Owner |
Florian Bayersdorfer |
Database submission license |
Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International |
Created by |
Florian Bayersdorfer |
Date created |
2024-09-09 10:19:36 +00:00 (UTC) |
Date last edited |
N/A |
Variant on transcripts
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