Variant #0000888146 (NC_000008.10:g.126091044G>A, NM_014846.3:c.647C>T (KIAA0196))
Chromosome |
8 |
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.126091044G>A |
DNA change (hg38) |
- |
Published as |
KIAA0196(NM_014846.3):c.647C>T (p.P216L, p.(Pro216Leu)), WASHC5(NM_014846.4):c.647C>T (p.P216L) |
ISCN |
- |
DB-ID |
KIAA0196_000030 See all 4 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) |
0.00111 View details |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2022-11-01 13:01:21 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
|