Full data view for gene OLFM1

Information The variants shown are described using the NM_014279.4 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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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.97-3659G>C r.(?) p.(=) Unknown ACMG VUS g.137978382G>C g.135086536G>C - - OLFM1_000002 - - - - De novo - 1/12 of patients - - - DNA MS, SEQ-NG-I blood WGS ADHD 329C - - M ? Hong Kong Chinese - - - - 1 Larry Baum
-?/. - c.97-2099A>C r.(=) p.(=) Unknown - likely benign g.137979942A>C g.135088096A>C OLFM1(NM_001282611.1):c.107A>C (p.K36T) - OLFM1_000001 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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