Full data view for gene AR

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

3 entries on 1 page. Showing entries 1 - 3.
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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     
+/. 1 c.521T>G - r.(?) p.(Leu174*) N-term Bmax zero Parent #1 - pathogenic g.66765509T>G g.67545667T>G 1636T>G - AR_000134 - PubMed: Gottlieb 1999 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
+/. 1 c.521T>G - r.(?) p.(Leu174*) N-term - Parent #1 - pathogenic g.66765509T>G g.67545667T>G 1636T>G - AR_000134 - PubMed: Hiort 1996 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
+/. 1 c.521T>G - r.(?) p.(Leu174*) N-term Bmax low; kD normal Parent #1 - pathogenic g.66765509T>G g.67545667T>G 1636T>G - AR_000134 - Holterhus et al. J Clin Endocrinol. 82: 3584- 3589, 1997 - - Somatic - - - - - DNA SEQ - - PAIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
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