All variants in the OBSL1 gene

Information The variants shown are described using the NM_001173408.1 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
Legend   How to query  

Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Classification method     

Clinical classification     

DNA change (genomic) (hg19)     

DNA change (hg38)     

Published as     

ISCN     

DB-ID     

Variant remarks     

Reference     

ClinVar ID     

dbSNP ID     

Origin     

Segregation     

Frequency     

Re-site     

VIP     

Methylation     

Owner     
-/. - c.1102C>T r.(?) p.(Arg368Cys) - benign g.220432957G>A g.219568235G>A OBSL1(NM_001173408.1):c.1102C>T (p.(Arg368Cys)) - OBSL1_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - 0 - VKGL-NL_Nijmegen
-?/. - c.1102C>T r.(?) p.(Arg368Cys) - likely benign g.220432957G>A g.219568235G>A OBSL1(NM_001173408.1):c.1102C>T (p.(Arg368Cys)) - OBSL1_000017 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - VKGL-NL_Leiden
-?/. - c.1102C>T r.(?) p.(Arg368Cys) - likely benign g.220432957G>A g.219568235G>A - - OBSL1_000017 61 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs35009641 Germline - 61/2795 individuals - 0 - Mohammed Faruq
Legend   How to query