Variant #0000677732 (NC_000006.11:g.31933780G>A, NM_006929.4:c.2192G>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.31933780G>A
DNA change (hg38) -
Published as SKIC2(NM_006929.5):c.2192G>A (p.R731H)
ISCN -
DB-ID DOM3Z_000013
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2020-08-06 14:59:34 +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.-7120C>T r.(?) p.(=)
STK19 NM_004197.1 ?/. - c.-5994G>A r.(?) p.(=)
DOM3Z NM_005510.3 ?/. - c.*3874C>T r.(=) p.(=)
SKIV2L NM_006929.4 ?/. - c.2192G>A r.(?) p.(Arg731His)


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