Variant #0000976064 (NC_000004.11:g.110681492_110681493del, NM_000204.3:c.816_817del (CFI))

Chromosome 4
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110681492_110681493del
DNA change (hg38) -
Published as CFI(NM_000204.5):c.816_817del (p.(Pro273Lysfs*8)), CFI(NM_001318057.1):c.816_817delTC (p.P273Kfs*8)
ISCN -
DB-ID CFI_000030 See all 2 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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
CFI NM_000204.3 +?/. - c.816_817del r.(?) p.(Pro273LysfsTer8)


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