Full data view for gene OBSL1

Information The variants shown are described using the NM_015311.2 transcript reference sequence.

3 entries on 1 page. Showing entries 1 - 3.
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Effect     

Exon     

AscendingDNA change (cDNA)     

RNA change     

Protein     

Allele     

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     

Template     

Technique     

Tissue     

Remarks     

Disease     

ID_report     

Reference     

Remarks     

Gender     

Consanguinity     

Country     

Population     

Age at death     

VIP     

Data_av     

Treatment     

Panel size     

Owner     
-?/. - c.3649G>A r.(?) p.(Glu1217Lys) Unknown - likely benign g.220422686C>T g.219557964C>T OBSL1(NM_001173408.1):c.*3920G>A (p.(=)), OBSL1(NM_015311.3):c.3649G>A (p.E1217K) - OBSL1_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-/. - c.3649G>A r.(?) p.(Glu1217Lys) Unknown - benign g.220422686C>T g.219557964C>T OBSL1(NM_001173408.1):c.*3920G>A (p.(=)), OBSL1(NM_015311.3):c.3649G>A (p.E1217K) - OBSL1_000035 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.3649G>A r.(?) p.(Glu1217Lys) Parent #1 - VUS g.220422686C>T g.219557964C>T - - OBSL1_000035 conflicting interpretations of pathogenicity; 12 heterozygous, no homozygous; Clinindb (India) PubMed: Narang 2020, Journal: Narang 2020 - rs72957510 Germline - 12/2789 individuals - 0 - DNA arraySNP - Infinium Global Screening Array v1.0 ? - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - 0 - - 12 Mohammed Faruq
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