Variant #0000895548 (NC_000021.8:g.47545690G>A, NC_000021.8(NM_001849.3):c.1970-9G>A (COL6A2))
Chromosome |
21 |
Allele |
Unknown |
Affects function (as reported) |
Affects function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
pathogenic |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.47545690G>A |
DNA change (hg38) |
- |
Published as |
COL6A2(NM_001849.3):c.1970-9G>A (p.?), COL6A2(NM_058175.2):c.1970-9G>A, COL6A2(NM_058175.3):c.1970-9G>A |
ISCN |
- |
DB-ID |
COL6A2_000056 See all 25 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) |
0.00011 View details |
Owner |
VKGL-NL_Utrecht |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Utrecht |
Date created |
2022-11-01 13:41:49 +01:00 (CET) |
Date last edited |
2024-08-28 13:16:32 +02:00 (CEST) |

Variant on transcripts
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