Full data view for gene AR

Information The variants shown are described using the NM_000044.3 transcript reference sequence.

2 entries on 1 page. Showing entries 1 - 2.
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Effect     

Exon     

AscendingDNA change (cDNA)     

Haplotype     

RNA change     

Protein     

P-domain     

Enzyme activity     

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     
+/. 4 c.2044G>T - r.(?) p.(Glu682*) LBD Bmax v low Parent #1 - pathogenic g.66931402G>T g.67711560G>T 3159G>T - AR_000276 - PubMed: MacLean 2004 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
+/. 4 c.2044G>T - r.(?) p.(Glu682*) LBD Bmax low Parent #1 - pathogenic g.66931402G>T g.67711560G>T 3159G>T - AR_000276 - PubMed: MacLean 2004 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
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