Variant #0000346662 (NC_000001.10:g.196762489_196762490del, NM_021023.5:c.839_840del (CFHR3))

Chromosome 1
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.196762489_196762490del
DNA change (hg38) g.196793359_196793360del
Published as CFHR3(NM_001166624.1):c.655_656del (p.(Ile219LysfsTer7))
ISCN -
DB-ID CFHR3_000017
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_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFHR3 NM_021023.5 -/. - c.839_840del r.(?) p.(Ile280LysfsTer7)


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