Variant #0000911962 (NC_000003.11:g.49064190A>G, NM_017730.2:c.*3695T>C (QRICH1))
Chromosome |
3 |
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.49064190A>G |
DNA change (hg38) |
- |
Published as |
IMPDH2(NM_000884.3):c.749T>C (p.I250T) |
ISCN |
- |
DB-ID |
IMPDH2_000011 |
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 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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