Variant #0000520574 (NC_000003.11:g.63898397_63898399dup, NM_000333.3:c.123_125dup (ATXN7))
Chromosome |
3 |
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.63898397_63898399dup |
DNA change (hg38) |
g.63912721_63912723dup |
Published as |
ATXN7(NM_000333.4):c.123_125dupGCC (p.P43dup), ATXN7(NM_001377405.1):c.123_125dup (p.(Pro43dup)) |
ISCN |
- |
DB-ID |
ATXN7_000049 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_AMC |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_AMC |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|