Variant #0000677727 (NC_000006.11:g.31915533G>A, NM_006929.4:c.-11437G>A (SKIV2L))

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.31915533G>A
DNA change (hg38) -
Published as CFB(NM_001710.5):c.673G>A (p.D225N)
ISCN -
DB-ID C2_000037
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) 1.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
Date last edited 2020-09-15 15:50:26 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 ?/. - c.*2399G>A r.(=) p.(=)
CFB NM_001710.5 ?/. - c.673G>A r.(?) p.(Asp225Asn)
NELFE NM_002904.5 ?/. - c.*4545C>T r.(=) p.(=)
SKIV2L NM_006929.4 ?/. - c.-11437G>A r.(?) p.(=)
ZBTB12 NM_181842.2 ?/. - c.-45940C>T r.(?) p.(=)


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