Variant #0000528325 (NC_000006.11:g.31931919_31931928del, NC_000006.11(NM_006929.4):c.1860+17_1860+26del (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.31931919_31931928del
DNA change (hg38) g.31964142_31964151del
Published as SKIV2L(NM_006929.4):c.1860+17_1860+26delCTGTGTGCGT, SKIV2L(NM_006929.5):c.1860+17_1860+26delCTGTGTGCGT
ISCN -
DB-ID SKIV2L_000032 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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
NELFE NM_002904.5 -?/. - c.-5252_-5243del r.(?) p.(=)
SKIV2L NM_006929.4 -?/. - c.1860+17_1860+26del r.(=) p.(=)


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