Variant #0000610279 (NC_000006.11:g.31929758G>A, NM_006929.4:c.991G>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.31929758G>A
DNA change (hg38) g.31961981G>A
Published as SKIV2L(NM_006929.4):c.991G>A (p.A331T), SKIV2L(NM_006929.5):c.991G>A (p.(Ala331Thr))
ISCN -
DB-ID SKIV2L_000033 See all 2 reported entries
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) 0.00012 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 ?/. - c.-3098C>T r.(?) p.(=)
SKIV2L NM_006929.4 ?/. - c.991G>A r.(?) p.(Ala331Thr)


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