Product Details

SNP ID

rs148354979

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:50966281 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTTTCCCATGGGCTCACTCATT[A/G]CCATACATCACTTGCCACACTATCA

Phenotype

MIM: 605430

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SPAG9 PubMed Links

Additional Information

For this assay, SNP(s) [rs9896965] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SPAG9

Gene Name

sperm associated antigen 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001130527.2	4205	Silent Mutation	GGC,GGT	G1309G	NP_001123999.1
NM_001130528.2	4205	Silent Mutation	GGC,GGT	G1319G	NP_001124000.1
NM_001251971.1	4205	Silent Mutation	GGC,GGT	G1175G	NP_001238900.1
NM_003971.5	4205	Silent Mutation	GGC,GGT	G1305G	NP_003962.3
XM_005257768.2	4205	Silent Mutation	GGC,GGT	G1332G	XP_005257825.1
XM_005257771.2	4205	Silent Mutation	GGC,GGT	G1318G	XP_005257828.1
XM_005257774.3	4205	Silent Mutation	GGC,GGT	G1162G	XP_005257831.1
XM_017025283.1	4205	Silent Mutation	GGC,GGT	G1189G	XP_016880772.1
XM_017025284.1	4205	Silent Mutation	GGC,GGT	G1176G	XP_016880773.1
XM_017025285.1	4205	Silent Mutation	GGC,GGT	G1167G	XP_016880774.1

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