Variant #0000528326 (NC_000006.11:g.31933733T>C, NM_006929.4:c.2145T>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.31933733T>C
DNA change (hg38) g.31965956T>C
Published as SKIV2L(NM_006929.5):c.2145T>C (p.V715=)
ISCN -
DB-ID DOM3Z_000001
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) 2.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 -?/. - c.-7073A>G r.(?) p.(=)
STK19 NM_004197.1 -?/. - c.-6041T>C r.(?) p.(=)
DOM3Z NM_005510.3 -?/. - c.*3921A>G r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.2145T>C r.(?) p.(Val715=)


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