Search

  • お問い合わせ一覧​
  • クイックオーダー

System Message

OKCancel
LOADING ...
See other FSHR GT Assays ›
SNP ID:
rs6166
Gene
FSHR
Gene Name
Set Membership:
> HapMap > Validated
Chromosome Location:
Chr.2: 48962782 - 48962782 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

AGGGACAAGTATGTAAGTGGAACCA[C/T]TGGTGACTCTGGGAGCTGAAGAGCA

Assay ID C___2676874_10
Size
Availability Made To Order
Catalog # 4351379
Price
Your Price
Online offer:
Check your price ›

Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

 MIM: 136435

Literature Links:

 FSHR PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
G (0.41)
(0.59)
Caucasian
C (0.48)
(0.52)
CEPH (CEU)
G (0.40)
(0.60)
EAS
G (0.32)
(0.68)
African American
C (0.38)
(0.62)
YRI (Yoruba)
G (0.47)
(0.53)
SAS
G (0.45)
(0.55)
Chinese - Not Available JPT (Japanese)
G (0.35)
(0.65)
AFR
G (0.41)
(0.59)
Japanese - Not Available CHB (Han Chinese)
G (0.29)
(0.71)
EUR
G (0.45)
(0.55)
AMR
G (0.42)
(0.58)
FSHR - follicle stimulating hormone receptor
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_000145.3 1832 Missense Mutation AAT,AGT N,S 680 NP_000136.2
NM_181446.2 1832 Missense Mutation AAT,AGT N,S 654 NP_852111.2
XM_011532733.2 1832 Missense Mutation AAT,AGT N,S 714 XP_011531035.1
XM_011532734.2 1832 Missense Mutation AAT,AGT N,S 603 XP_011531036.1
XM_011532735.2 1832 Missense Mutation AAT,AGT N,S 416 XP_011531037.1
XM_011532736.2 1832 Missense Mutation AAT,AGT N,S 416 XP_011531038.1
XM_011532740.1 1832 Intron XP_011531042.1

Back To Top

Related Products