Variant #0000332930 (NC_000009.11:g.139906990C>T, NM_207511.1:c.-16440C>T (C9orf139))
Chromosome |
9 |
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.139906990C>T |
DNA change (hg38) |
g.137012538C>T |
Published as |
ABCA2(NM_001606.4):c.5134G>A (p.(Gly1712Ser)), ABCA2(NM_001606.5):c.5134G>A (p.G1712S), ABCA2(NM_212533.3):c.5224G>A (p.G1742S) |
ISCN |
- |
DB-ID |
ABCA2_000001 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) |
0.00324 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2024-02-26 20:06:56 +01:00 (CET) |

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