Variant #0000688052 (NC_000001.10:g.22965716G>A, NM_172369.3:c.-4505G>A (C1QC))

Chromosome 1
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.22965716G>A
DNA change (hg38) -
Published as C1QA(NM_001347465.1):c.554G>A (p.R185H)
ISCN -
DB-ID C1QA_000008
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QA NM_015991.2 -?/. - c.554G>A r.(?) p.(Arg185His)
C1QC NM_172369.3 -?/. - c.-4505G>A r.(?) p.(=)


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