Variant #0000887156 (NC_000006.11:g.31933730C>T, NM_006929.4:c.2142C>T (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.31933730C>T
DNA change (hg38) -
Published as SKIV2L(NM_006929.5):c.2142C>T (p.T714=)
ISCN -
DB-ID DOM3Z_000021
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) 3.0E-5 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 2022-11-01 13:01:21 +01:00 (CET)
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.-7070G>A r.(?) p.(=)
STK19 NM_004197.1 -?/. - c.-6044C>T r.(?) p.(=)
DOM3Z NM_005510.3 -?/. - c.*3924G>A r.(=) p.(=)
SKIV2L NM_006929.4 -?/. - c.2142C>T r.(?) p.(Thr714=)


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