Variant #0000322895 (NC_000012.11:g.53702572G>A, NM_015665.5:c.1024C>T (AAAS))
Chromosome |
12 |
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.53702572G>A |
DNA change (hg38) |
g.53308788G>A |
Published as |
AAAS(NM_001173466.1):c.925C>T (p.(Arg309Ter)), AAAS(NM_015665.5):c.1024C>T (p.R342*) |
ISCN |
- |
DB-ID |
AAAS_000004 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) |
1.0E-5 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 |
2020-07-02 16:03:32 +02:00 (CEST) |

Variant on transcripts
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