Variant #0000924033 (NC_000004.11:g.110662159C>G, NM_000204.3:c.1642G>C (CFI))

Chromosome 4
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.110662159C>G
DNA change (hg38) -
Published as CFI(NM_000204.3):c.1642G>C (p.E548Q), CFI(NM_000204.5):c.1642G>C (p.E548Q), CFI(NM_001318057.1):c.1666G>C (p.E556Q)
ISCN -
DB-ID CFI_000002 See all 4 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) 0.00072 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-04-16 21:50:28 +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.1642G>C r.(?) p.(Glu548Gln)


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