Variant #0000720840 (NC_000006.11:g.31963559A>G, NM_007293.2:c.3218A>G (C4A))

Chromosome 6
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.31963559A>G
DNA change (hg38) -
Published as C4A(NM_007293.2):c.3218A>G (p.D1073G), C4A(NM_007293.3):c.3218A>G (p.(Asp1073Gly))
ISCN -
DB-ID C4A_000014 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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C4A NM_007293.2 -?/. - c.3218A>G r.(?) p.(Asp1073Gly)


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