Variant #0000543911 (NC_000011.9:g.44117805G>A, NC_000011.9(NM_207122.1):c.-31+403G>A (EXT2))
Chromosome |
11 |
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.44117805G>A |
DNA change (hg38) |
g.44096255G>A |
Published as |
EXT2(NM_000401.3):c.3G>A (p.M1?) |
ISCN |
- |
DB-ID |
EXT2_000407 |
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) |
2.0E-5 View details |
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 |
2022-10-07 13:17:02 +02:00 (CEST) |

Variant on transcripts
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