Variant #0000851169 (NC_000006.11:g.31914847A>G, NM_000063.4:c.*1713A>G (C2))

Chromosome 6
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.31914847A>G
DNA change (hg38) -
Published as CFB(NM_001710.6):c.362A>G (p.Y121C)
ISCN -
DB-ID C2_000054
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) 7.0E-5 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 2022-05-09 15:40:45 +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.*1713A>G r.(=) p.(=)
CFB NM_001710.5 ?/. - c.362A>G r.(?) p.(Tyr121Cys)
ZBTB12 NM_181842.2 ?/. - c.-45254T>C r.(?) p.(=)


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