Variant #0000609089 (NC_000004.11:g.151829580T>C, NM_001199282.2:c.1399A>G (LRBA))
Chromosome |
4 |
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.151829580T>C |
DNA change (hg38) |
g.150908428T>C |
Published as |
LRBA(NM_001199282.2):c.1399A>G (p.(Met467Val), p.M467V), LRBA(NM_001367550.1):c.1399A>G (p.M467V) |
ISCN |
- |
DB-ID |
LRBA_000096 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) |
0.00211 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
|
Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.
|