Full data view for gene AR

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

5 entries on 1 page. Showing entries 1 - 5.
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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     
+/+ 8 c.2659A>G - r.(?) p.(Met887Val) LBD Bmax normal; kD normal; k normal Parent #1 - pathogenic g.66943579A>G g.67723737A>G 3774A>G - AR_000172 50% red. in transactivation PubMed: Ghadessy 1999 - - Germline - - - - - DNA SEQ - - MAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/+ 8 c.2659A>G - r.(?) p.(Met887Val) LBD Bmax normal; kD normal; k normal Parent #1 - pathogenic g.66943579A>G g.67723737A>G 3774A>G - AR_000172 50% red. in transactivation PubMed: Ghadessy 1999 - - Germline - - - - - DNA SEQ - - MAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/+ 8 c.2659A>G - r.(?) p.(Met887Val) LBD - Parent #1 - pathogenic g.66943579A>G g.67723737A>G 3774A>G - AR_000172 - Yeh et al. Int J Cancer 120: 1610-1617, 2007 - - Somatic - - - - - DNA SEQ - - ? - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/. - c.2659A>G - r.(?) p.(Met887Val) - - Maternal (inferred) - pathogenic g.66943579A>G g.67723737A>G - 46,XY AR_000172 - PubMed: Eggers 2016 - - Germline - - - - - DNA SEQ-NG - 1031 gene panel DSD Pat125 PubMed: Eggers 2016 - - - - - - - - - 1 Johan den Dunnen
-?/. - c.2659A>G - r.(?) p.(Met887Val) - - Unknown - likely benign g.66943579A>G g.67723737A>G - - AR_000172 classification based on frequency in 305 unrelated individuals PubMed: Le 2019 - - Germline - frequency 0.013 - - - DNA SEQ, SEQ-NG - 105 WGS/200 WES Healthy/Control - PubMed: Le 2019 analysis 305 unrelated individuals - - Viet Nam - - - - - 1 Global Variome, with Curator vacancy
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