Variant #0000514971 (NC_000002.11:g.228163475G>A, NM_000091.4:c.3829G>A (COL4A3))
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.228163475G>A |
DNA change (hg38) |
g.227298759G>A |
Published as |
COL4A3(NM_000091.4):c.3829G>A (p.G1277S), COL4A3(NM_000091.5):c.3829G>A (p.(Gly1277Ser)) |
ISCN |
- |
DB-ID |
COL4A3_000085 See all 10 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 |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2024-04-19 20:20:39 +02:00 (CEST) |

Variant on transcripts
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