Variant #0000910727 (NC_000001.10:g.103491487T>A, NC_000001.10(NM_001854.3):c.897+285A>T (COL11A1))
Chromosome |
1 |
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.103491487T>A |
DNA change (hg38) |
- |
Published as |
COL11A1(NM_080629.2):c.802A>T (p.(Lys268*)) |
ISCN |
- |
DB-ID |
COL11A1_000359 |
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) |
1.0E-5 View details |
Owner |
VKGL-NL_Leiden |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Leiden |
Date created |
2023-01-11 15:44:22 +01:00 (CET) |
Date last edited |
N/A |

Variant on transcripts
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