Full data view for gene AR

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

15 entries on 1 page. Showing entries 1 - 15.
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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.1174C>T - r.(?) p.(Pro392Ser) N-term Bmax normal; kD normal Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - PubMed: Audi 2010 - - Germline - - - - - DNA SEQ - - PAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/. 1 c.1174C>T - r.(?) p.(Pro392Ser) LBD Bmax normal; kD high Unknown - pathogenic g.66766162C>T g.67546320C>T - - AR_000218 - PubMed: Boehmer 2001 - - Germline - - - - - DNA SEQ - - PAIS - - sex of rearing F; niece of 0745 rF - - - - - - - 1 Bruce Gottlieb
+/. 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term - Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - PubMed: Ferlin 2006 - - Germline - - - - - DNA SEQ - - INFM - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/+ 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term - Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - PubMed: Hiort 2000 - - Germline - - - - - DNA SEQ - - MAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/+ 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term - Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - PubMed: Hiort 2000 - - Germline - - - - - DNA SEQ - - MAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/. 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term Bmax zero Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - Appari et al. J Molecular Med: 87: 623-632, 2009 - - Germline - - - - - DNA SEQ - - AIS - - sex of rearing F rF - - - - - - - 1 Bruce Gottlieb
+/. 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term - Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - Bhangoo et al. Asian J Androl 12: 561-566. 2010 - - Germline - - - - - DNA SEQ - - PAIS - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
+/. 1 c.1174C>T - r.(?) p.(Pro392Ser) N-term - Parent #1 - pathogenic g.66766162C>T g.67546320C>T 2289C>T - AR_000218 - Garolla et al. Encdorine Related Cancer 12: 645-655, 2005 - - Somatic - - - - - DNA SEQ - - ? - - sex of rearing M rM - - - - - - - 1 Bruce Gottlieb
-?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Unknown - likely benign g.66766162C>T g.67546320C>T AR(NM_000044.3):c.1174C>T (p.(Pro392Ser)), AR(NM_000044.4):c.1174C>T (p.P392S), AR(NM_000044.6):c.1174C>T (p.P392S) - AR_000218 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
-?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Unknown - likely benign g.66766162C>T g.67546320C>T AR(NM_000044.3):c.1174C>T (p.(Pro392Ser)), AR(NM_000044.4):c.1174C>T (p.P392S), AR(NM_000044.6):c.1174C>T (p.P392S) - AR_000218 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Maternal (confirmed) - VUS g.66766162C>T g.67546320C>T - - AR_000218 - PubMed: Mavros 2018 - rs201934623 Germline - - - - - DNA SEQ, SEQ-NG - trio WES ID PAt1 PubMed: Mavros 2018 - M no United States - - - - - 1 Johan den Dunnen
+/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Maternal (inferred) - pathogenic g.66766162C>T g.67546320C>T - 46,XY AR_000218 - PubMed: Eggers 2016 - - Germline - - - - - DNA SEQ-NG - 1031 gene panel DSD Pat67 PubMed: Eggers 2016 - - - - - - - - - 1 Johan den Dunnen
+?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Both (homozygous) - likely pathogenic g.66766162C>T g.67546320C>T c.1174C>T , P392S - AR_000218 Homozygous PubMed: Chakrabarty 2020 - - Germline yes - - - - DNA SEQ-NG-IT, SEQ blood whole exome sequencing retinal disease II:1 PubMed: Chakrabarty 2020 - M - India - - - - - 1 LOVD
+?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Both (homozygous) - likely pathogenic g.66766162C>T g.67546320C>T c.1174C>T , P392S - AR_000218 Homozygous PubMed: Chakrabarty 2020 - - Germline yes - - - - DNA SEQ-NG-IT, SEQ blood whole exome sequencing retinal disease II:2 PubMed: Chakrabarty 2020 - M - India - - - - - 1 LOVD
-?/. - c.1174C>T - r.(?) p.(Pro392Ser) - - Unknown - likely benign g.66766162C>T - AR(NM_000044.3):c.1174C>T (p.(Pro392Ser)), AR(NM_000044.4):c.1174C>T (p.P392S), AR(NM_000044.6):c.1174C>T (p.P392S) - AR_000218 VKGL data sharing initiative Nederland - - - CLASSIFICATION record - - - - - - - - - - - - - - - - - - - - - - -
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