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SNP ID:
rs9992086
Gene
STPG2 STPG2-AS1
Gene Name
Set Membership:
> HapMap
Chromosome Location:
Chr.4: 97480597 - 97480597 on Build GRCh38
Polymorphism:
C/T, Transition substitution
Context Sequence [VIC/FAM]:

GAGAGTATCAGTTGCTATTAATCAT[C/T]AATACTGGATATTTTCTTTTTAATT

Assay ID C__30592405_10
Size
Availability Made To Order
Catalog # 4351379
Price
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Assay Details



Species:

 Human

dbSNP Submissions:

 NA

Phenotype:

Literature Links:

 STPG2 PubMed Links

Allele Nomenclature:

Minor Allele Frequency:
1000Genome Applied Biosystems® HapMap
Global
C (0.19)
(0.81)
Caucasian - Not Available CEPH (CEU)
C (0.03)
(0.97)
EAS
C (0.10)
(0.90)
African American - Not Available YRI (Yoruba)
T (0.49)
(0.51)
SAS
C (0.08)
(0.92)
Chinese - Not Available JPT (Japanese)
C (0.12)
(0.88)
AFR
C (0.50)
(0.50)
Japanese - Not Available CHB (Han Chinese)
C (0.15)
(0.85)
EUR
C (0.06)
(0.94)
AMR
C (0.09)
(0.91)
STPG2 - sperm tail PG-rich repeat containing 2
Transcript Accession SNP Location SNP Type Observed Codons Observed Amino Acid Protein ID
NM_174952.2 Intron NP_777612.1
XM_011531886.2 Intron XP_011530188.1
XM_017008049.1 Intron XP_016863538.1
XM_017008050.1 Intron XP_016863539.1
XM_017008051.1 Intron XP_016863540.1
STPG2-AS1 - STPG2 antisense RNA 1
There are no transcripts associated with this gene.

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More Information


Set Membership:

 HapMap

Panther Classification:

Molecular Function -

structural protein

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