Variant #0000658920 (NC_000022.10:g.29454756A>G, NM_001206998.1:c.*5146A>G (ZNRF3))
Chromosome |
22 |
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.29454756A>G |
DNA change (hg38) |
g.29058768A>G |
Published as |
C22orf31(NM_015370.1):c.847T>C (p.W283R) |
ISCN |
- |
DB-ID |
C22orf31_000001 |
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_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2020-03-23 16:13:27 +01:00 (CET) |
Date last edited |
2024-10-29 21:08:56 +01:00 (CET) |

Variant on transcripts
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