Variant #0000802505 (NC_000006.11:g.31929148A>G, NM_006929.4:c.774A>G (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.31929148A>G
DNA change (hg38) -
Published as SKIV2L(NM_006929.5):c.774A>G (p.E258=)
ISCN -
DB-ID SKIV2L_000042
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) 0.00254 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 -?/. - c.-2488T>C r.(?) p.(=)
SKIV2L NM_006929.4 -?/. - c.774A>G r.(?) p.(Glu258=)


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