Variant #0000527952 (NC_000006.11:g.16327903_16327908dup, NM_000332.3:c.672_677dup (ATXN1))
Chromosome |
6 |
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.16327903_16327908dup |
DNA change (hg38) |
g.16327672_16327677dup |
Published as |
ATXN1(NM_000332.3):c.672_677dupGCAGCA (p.Q224_Q225dup) |
ISCN |
- |
DB-ID |
ATXN1_000041 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_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
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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