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 InternationalCreative Commons License
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)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4A NM_007293.2 +/. - c.3694_3695dup r.(?) p.(Val1233GlnfsTer75)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.