Variant #0000272254 (NC_000001.10:g.22970567_22970569del, NM_172369.3:c.51_53del (C1QC))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.22970567_22970569del
DNA change (hg38) g.22644074_22644076del
Published as C1QC(NM_001114101.1):c.51_53delGCT (p.L22del)
ISCN -
DB-ID C1QC_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C1QA NM_015991.2 ?/. - c.*4667_*4669del r.(=) p.(=)
C1QC NM_172369.3 ?/. - c.51_53del r.(?) p.(Leu22del)


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