Variant #0000526217 (NC_000005.9:g.82817656T>C, NM_004385.4:c.3531T>C (VCAN))
Chromosome |
5 |
Allele |
Unknown |
Affects function (as reported) |
Probably does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
likely benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.82817656T>C |
DNA change (hg38) |
g.83521837T>C |
Published as |
VCAN(NM_004385.4):c.3531T>C (p.D1177=) |
ISCN |
- |
DB-ID |
VCAN_000101 |
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_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 |
2020-06-17 11:50:21 +02:00 (CEST) |

Variant on transcripts
|