Variant #0000925929 (NC_000014.8:g.92537354_92537355insTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG, NM_004993.5:c.915_916insCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA (ATXN3))
Chromosome |
14 |
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.92537354_92537355insTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTGCTG |
DNA change (hg38) |
- |
Published as |
ATXN3(NM_004993.6):c.915_916ins41 (p.G306Qfs*39), ATXN3(NM_004993.6):c.915_916insCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCAGCA (p.(Gly306GlnfsTer39)) |
ISCN |
- |
DB-ID |
ATXN3_000087 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_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-04-16 21:50:28 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
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