Variant #0000291081 (NC_000018.9:g.2929103G>A, NM_014646.2:c.1510C>T (LPIN2))
Chromosome |
18 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.2929103G>A |
DNA change (hg38) |
g.2929105G>A |
Published as |
LPIN2(NM_001375808.2):c.1510C>T (p.(Leu504Phe)), LPIN2(NM_014646.2):c.1510C>T (p.L504F) |
ISCN |
- |
DB-ID |
LPIN2_000015 See all 5 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) |
0.00262 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2025-05-05 21:14:00 +02:00 (CEST) |

Variant on transcripts
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