Variant #0000804219 (NC_000009.11:g.94495533T>C, NM_004560.3:c.808A>G (ROR2))
Chromosome |
9 |
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.94495533T>C |
DNA change (hg38) |
- |
Published as |
ROR2(NM_004560.4):c.808A>G (p.I270V) |
ISCN |
- |
DB-ID |
ROR2_000080 |
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) |
0.00017 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2021-09-17 14:40:49 +02:00 (CEST) |
Date last edited |
N/A |

Variant on transcripts
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