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     
+/. 2 c.1771A>G - r.spl? p.(Lys591Glu) - - Unknown - pathogenic g.66905854A>G g.67686012A>G - - AR_000378 - PubMed: Audi 2010 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
+/. 2 c.1771A>G - r.(?) p.(Lys591Glu) - - Parent #1 - pathogenic g.66905854A>G g.67686012A>G - - AR_000378 - PubMed: Audi 2010 - - Germline - - - - - DNA SEQ - - AIS 19377374-Pat? PubMed: Tarpey 2009 - - - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - 1 Lucy Raymond
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