C_176793835_10

• SNP ID: rs181599171
• Gene: SPATA9
• Gene Name: spermatogenesis associated 9
• Set Membership: -
• Chromosome Location: Chr.5: 95695635 - 95695635 on Build GRCh38
• Polymorphism: T/G, Transversion substitution
• Context Sequence [VIC/FAM]:

  ACAAACAAACACATTTACACTCTTA[T/G]ATATTGTTGAGAACTCCCTAATAGC

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:	MIM: 608039
Literature Links:	SPATA9 PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

1000Genome	Applied Biosystems^®	HapMap
Global G (0.00) (1.00)	Caucasian - Not Available	CEPH (CEU) - Not Available
EAS G (0.00) (1.00)	African American - Not Available	YRI (Yoruba) - Not Available
SAS G (0.00) (1.00)	Chinese - Not Available	CHB (Han Chinese) - Not Available
AFR G (0.01) (0.99)	Japanese - Not Available	JPT (Japanese) - Not Available
EUR G (0.00) (1.00)
AMR G (0.00) (1.00)

SPATA9 - spermatogenesis associated 9
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_031952.3		Intron			NP_114158.2
XM_011543664.1		Intron			XP_011541966.1
XM_011543666.1		Intron			XP_011541968.1
XM_011543667.2		Intron			XP_011541969.1
XM_017009948.1		Intron			XP_016865437.1
XM_017009949.1		Intron			XP_016865438.1
XM_017009950.1		Intron			XP_016865439.1
XM_017009951.1		Intron			XP_016865440.1

More Information

Gene Ontology Categories:

Process(es)

multicellular organism development
spermatogenesis
cell differentiation