Variant #0000308199 (NC_000006.11:g.31928039C>G, NM_006929.4:c.279C>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.31928039C>G
DNA change (hg38) g.31960262C>G
Published as SKIV2L(NM_006929.4):c.279C>G (p.V93=)
ISCN -
DB-ID SKIV2L_000010
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) 0.0039 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 17:12:27 +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.-1379G>C r.(?) p.(=)
SKIV2L NM_006929.4 -?/. - c.279C>G r.(?) p.(Val93=)


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