Variant #0000564833 (NC_000018.9:g.43505732T>C, NM_020964.2:c.2690A>G (EPG5))
Chromosome |
18 |
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.43505732T>C |
DNA change (hg38) |
g.45925766T>C |
Published as |
EPG5(NM_020964.2):c.2690A>G (p.(Glu897Gly)), EPG5(NM_020964.3):c.2690A>G (p.E897G) |
ISCN |
- |
DB-ID |
EPG5_000031 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2019-12-04 15:24:38 +01:00 (CET) |

Variant on transcripts
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