Variant #0000677735 (NC_000006.11:g.31938176C>T, NM_006929.4:c.*684C>T (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.31938176C>T
DNA change (hg38) -
Published as DXO(NM_005510.4):c.892G>A (p.G298S)
ISCN -
DB-ID DOM3Z_000015
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_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)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 ?/. - c.-11516G>A r.(?) p.(=)
STK19 NM_004197.1 ?/. - c.-1598C>T r.(?) p.(=)
DOM3Z NM_005510.3 ?/. - c.892G>A r.(?) p.(Gly298Ser)
SKIV2L NM_006929.4 ?/. - c.*684C>T r.(=) p.(=)


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