Variant #0000528312 (NC_000006.11:g.31918468A>C, NM_006929.4:c.-8502A>C (SKIV2L))

Chromosome 6
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.31918468A>C
DNA change (hg38) g.31950691A>C
Published as CFB(NM_001710.5):c.1697A>C (p.E566A)
ISCN -
DB-ID CFB_000011 See all 5 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) 0.01121 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CFB NM_001710.5 -?/. - c.1697A>C r.(?) p.(Glu566Ala)
NELFE NM_002904.5 -?/. - c.*1610T>G r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.-8502A>C r.(?) p.(=)


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