Variant #0000521167 (NC_000004.11:g.110681505C>T, NM_000204.3:c.804G>A (CFI))

Chromosome 4
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.110681505C>T
DNA change (hg38) g.109760349C>T
Published as CFI(NM_000204.3):c.804G>A (p.S268=), CFI(NM_000204.5):c.804G>A (p.S268=)
ISCN -
DB-ID CFI_000021 See all 3 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) 0.29204 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFI NM_000204.3 -/. - c.804G>A r.(?) p.(Ser268=)


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