Variant #0000528345 (NC_000006.11:g.31964623_31964624dup, NM_007293.2:c.3694_3695dup (C4A))
Chromosome |
6 |
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.31964623_31964624dup |
DNA change (hg38) |
g.31996846_31996847dup |
Published as |
C4A(NM_001252204.1):c.3692_3693insCT (p.(Val1233GlnfsTer75)), C4A(NM_007293.3):c.3694_3695dupTC (p.V1233Qfs*75) |
ISCN |
- |
DB-ID |
C4A_000001 See all 3 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) |
Retrieve |
Owner |
VKGL-NL_Groningen |
Database submission license |
Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International |
Created by |
VKGL-NL_Groningen |
Date created |
2019-07-18 18:22:55 +02:00 (CEST) |
Date last edited |
2023-01-11 15:44:22 +01:00 (CET) |

Variant on transcripts
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