Product Details

SNP ID

rs139767835

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.X:67545280 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCGGGCCCCAGGCACCCAGAGGCCG[C/G]GAGCGCAGCACCTCCCGGCGCCAGT

Phenotype

MIM: 313700

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

AR PubMed Links

Gene Details

Gene

AR

Gene Name

androgen receptor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000044.3	1249	Missense Mutation	GCG,GGG	A45G	NP_000035.2
NM_001011645.2	1249	Intron			NP_001011645.1

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