Variant #0000572024 (NC_000022.10:g.38379688_38379690dup, NM_006941.3:c.114_116dup (SOX10))
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.38379688_38379690dup |
DNA change (hg38) |
g.37983681_37983683dup |
Published as |
SOX10(NM_006941.3):c.114_116dupCGG (p.G39dup), SOX10(NM_006941.4):c.114_116dup (p.(Gly39dup)) |
ISCN |
- |
DB-ID |
SOX10_000118 See all 2 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) |
Retrieve |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:27:30 +02:00 (CEST) |

Variant on transcripts
|