Variant #0000607691 (NC_000002.11:g.228102752C>A, NC_000002.11(NM_000091.4):c.144+12C>A (COL4A3))
Chromosome |
2 |
Allele |
Unknown |
Affects function (as reported) |
Does not affect function |
Affects function (by curator) |
Not classified |
Classification method |
- |
Clinical classification |
benign |
DNA change (genomic) (Relative to hg19 / GRCh37) |
g.228102752C>A |
DNA change (hg38) |
g.227238036C>A |
Published as |
COL4A3(NM_000091.5):c.144+12C>A, MFF-DT(NR_102371.1):n.1681+50G>T |
ISCN |
- |
DB-ID |
COL4A3_000006 See all 6 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) |
0.30926 View details |
Owner |
VKGL-NL_Nijmegen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Nijmegen |
Date created |
2019-12-04 14:54:23 +01:00 (CET) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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