Variant #0000802500 (NC_000006.11:g.31916231A>C, NM_006929.4:c.-10739A>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.31916231A>C
DNA change (hg38) -
Published as CFB(NM_001710.5):c.978A>C (p.E326D)
ISCN -
DB-ID C2_000049
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) 0.00071 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 -?/. - c.*3097A>C r.(=) p.(=)
CFB NM_001710.5 -?/. - c.978A>C r.(?) p.(Glu326Asp)
NELFE NM_002904.5 -?/. - c.*3847T>G r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.-10739A>C r.(?) p.(=)
ZBTB12 NM_181842.2 -?/. - c.-46638T>G r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.