Variant #0000560291 (NC_000017.10:g.1265317dup, NC_000017.10(NM_006761.4):c.265-3dup (YWHAE))
Chromosome |
17 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.1265317dup |
DNA change (hg38) |
g.1362023dup |
Published as |
YWHAE(NM_006761.4):c.265-3dupT |
ISCN |
- |
DB-ID |
YWHAE_000010 |
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 |
2020-07-10 18:22:43 +02:00 (CEST) |

Variant on transcripts
|