Variant #0000886935 (NC_000005.9:g.89989752C>T, NM_032119.3:c.7179C>T (GPR98))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.89989752C>T |
DNA change (hg38) |
- |
Published as |
ADGRV1(NM_032119.4):c.7179C>T (p.D2393=) |
ISCN |
- |
DB-ID |
GPR98_000119 See all 5 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) |
0.00836 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|