Variant #0000528297 (NC_000006.11:g.31915580G>A, NM_006929.4:c.-11390G>A (SKIV2L))

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.31915580G>A
DNA change (hg38) g.31947803G>A
Published as -
ISCN -
DB-ID C2_000017
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_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 2020-06-18 17:04:04 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
C2 NM_000063.4 -/. - c.*2446G>A r.(=) p.(=)
CFB NM_001710.5 -/. - c.720G>A r.(?) p.(Glu240=)
NELFE NM_002904.5 -/. - c.*4498C>T r.(=) p.(=)
SKIV2L NM_006929.4 -/. - c.-11390G>A r.(?) p.(=)
ZBTB12 NM_181842.2 -/. - c.-45987C>T r.(?) p.(=)


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