Variant #0000514861 (NC_000002.11:g.220435437del, NM_015311.2:c.518del (OBSL1))

Chromosome 2
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.220435437del
DNA change (hg38) g.219570715del
Published as OBSL1(NM_001173408.1):c.518delA (p.(Asp173AlafsTer85))
ISCN -
DB-ID INHA_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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2022-11-01 13:01:21 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
INHA NM_002191.3 ?/. - c.-1660del r.(?) p.(=)
OBSL1 NM_015311.2 ?/. - c.518del r.(?) p.(Asp173AlafsTer85)


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