Variant #0000528295 (NC_000006.11:g.31914024T>A, NM_000063.4:c.*890T>A (C2))

Chromosome 6
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.31914024T>A
DNA change (hg38) g.31946247T>A
Published as CFB(NM_001710.5):c.26T>A (p.(Leu9His), p.L9H), CFB(NM_001710.6):c.26T>A (p.L9H)
ISCN -
DB-ID CFB_000001 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) 0.03909 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 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     
C2 NM_000063.4 -/. - c.*890T>A r.(=) p.(=)
CFB NM_001710.5 -/. - c.26T>A r.(?) p.(Leu9His)
ZBTB12 NM_181842.2 -/. - c.-44431A>T r.(?) p.(=)


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