Variant #0000308198 (NC_000006.11:g.31935145G>A, NM_006929.4:c.2574G>A (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.31935145G>A
DNA change (hg38) g.31967368G>A
Published as SKIV2L(NM_006929.4):c.2574G>A (p.V858=)
ISCN -
DB-ID SKIV2L_000020
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) 0.00298 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-18 17:17:01 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 -?/. - c.-8485C>T r.(?) p.(=)
STK19 NM_004197.1 -?/. - c.-4629G>A r.(?) p.(=)
DOM3Z NM_005510.3 -?/. - c.*2509C>T r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.2574G>A r.(?) p.(Val858=)


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