Variant #0000680992 (NC_000017.10:g.66547263T>G, NC_000017.10(NM_017565.3):c.719+751A>C (FAM20A))
Chromosome |
17 |
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.66547263T>G |
DNA change (hg38) |
- |
Published as |
PRKAR1A(NM_001276290.1):c.1012T>G (p.*338Eext*7, p.(*338Gluext*7)) |
ISCN |
- |
DB-ID |
FAM20A_000030 See all 2 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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-08-06 14:59:34 +02:00 (CEST) |
Date last edited |
2023-04-16 21:50:28 +02:00 (CEST) |

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