Variant #0000849803 (NC_000002.11:g.238289917C>T, NM_004369.3:c.1538G>A (COL6A3))
Chromosome |
2 |
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.238289917C>T |
DNA change (hg38) |
- |
Published as |
COL6A3(NM_004369.3):c.1538G>A (p.R513Q, p.(Arg513Gln)), COL6A3(NM_004369.4):c.1538G>A (p.R513Q) |
ISCN |
- |
DB-ID |
COL6A3_000483 See all 8 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) |
0.00038 View details |
Owner |
VKGL-NL_Rotterdam |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Rotterdam |
Date created |
2022-05-09 15:40:45 +02:00 (CEST) |
Date last edited |
2024-10-29 20:49:11 +01:00 (CET) |

Variant on transcripts
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