C_101300431_10

• SNP ID: rs79625181
• Gene: SPATA6L
• Gene Name: spermatogenesis associated 6 like
• Set Membership: -
• Chromosome Location: Chr.9: 4642881 - 4642881 on Build GRCh38
• Polymorphism: T/C, Transition substitution
• Context Sequence [VIC/FAM]:

  TCAAAGGACAGTGACAGTCACTTTA[T/C]ACAGAAGGAAAGAAAGAAAACAAAT

Assay Details

Species:	Human
dbSNP Submissions:	NA
Phenotype:
Literature Links:	SPATA6L PubMed Links
Allele Nomenclature:
Minor Allele Frequency:

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

SPATA6L - spermatogenesis associated 6 like
Transcript Accession	SNP Location	SNP Type	Observed Codons	Observed Amino Acid	Protein ID
NM_001039395.3		Intron			NP_001034484.3
XM_006716795.2		Intron			XP_006716858.1
XM_006716798.3		Intron			XP_006716861.1
XM_006716799.3		Intron			XP_006716862.1
XM_006716800.2		Intron			XP_006716863.1
XM_006716801.2		Intron			XP_006716864.1
XM_011517952.1		Intron			XP_011516254.1
XM_011517954.1		Intron			XP_011516256.1
XM_011517956.1		Intron			XP_011516258.1
XM_011517957.1		Intron			XP_011516259.1
XM_011517958.1		Intron			XP_011516260.1
XM_017014881.1		Intron			XP_016870370.1
XM_017014882.1		Intron			XP_016870371.1
XM_017014883.1		Intron			XP_016870372.1
XM_017014884.1		Intron			XP_016870373.1
XM_017014885.1		Intron			XP_016870374.1
XM_017014886.1		Intron			XP_016870375.1
XM_017014887.1		Intron			XP_016870376.1