Variant #0000514844 (NC_000002.11:g.220424170_220424184del, NM_015311.2:c.2998_3012del (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.220424170_220424184del
DNA change (hg38) g.219559448_219559462del
Published as OBSL1(NM_015311.3):c.2998_3012delATCGCCGTGACCTTG (p.I1000_L1004del)
ISCN -
DB-ID OBSL1_000040
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
OBSL1 NM_015311.2 ?/. - c.2998_3012del r.(?) p.(Ile1000_Leu1004del)


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