Variant #0000331224 (NC_000006.11:g.132859712_132859714del, NM_175057.3:c.284_286del (TAAR9))
Chromosome |
6 |
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.132859712_132859714del |
DNA change (hg38) |
g.132538573_132538575del |
Published as |
TAAR9(NM_175057.3):c.284_286del (p.(Glu95_Ser96delinsGly)) |
ISCN |
- |
DB-ID |
TAAR9_000002 |
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) |
0.00118 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2018-01-15 20:58:59 +01:00 (CET) |
Date last edited |
2020-06-22 10:24:34 +02:00 (CEST) |

Variant on transcripts
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