Variant #0000276580 (NC_000017.10:g.66538123C>A, NC_000017.10(NM_017565.3):c.1109+3G>T (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.66538123C>A |
DNA change (hg38) |
g.68541982C>A |
Published as |
FAM20A(NM_001243746.1):c.695+3G>T |
ISCN |
- |
DB-ID |
FAM20A_000006 |
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 |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-07-14 10:53:17 +02:00 (CEST) |

Variant on transcripts
|