Variant #0000611435 (NC_000008.10:g.126079895T>C, NM_014846.3:c.1217A>G (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.126079895T>C |
| DNA change (hg38) |
g.125067653T>C |
| Published as |
KIAA0196(NM_014846.3):c.1217A>G (p.N406S, p.(Asn406Ser)), WASHC5(NM_014846.4):c.1217A>G (p.N406S) |
| ISCN |
- |
| DB-ID |
KIAA0196_000020 See all 3 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) |
0.00011 View details |
| Owner |
VKGL-NL_Utrecht |
| Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
| Created by |
VKGL-NL_Utrecht |
| Date created |
2019-12-04 15:24:38 +01:00 (CET) |
| Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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