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SNP ID

rs74114932

Assay Type

Functionally tested

NCBI dbSNP Submissions

11

Location

Chr.1:117957008 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AATAATAAAGGGAAGGATTTAAAAA[C/T]TGACCATGTTAACAACGTTAACAAA

Phenotype

MIM: 616554 MIM: 604737

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SPAG17 PubMed Links

Gene Details

Gene

SPAG17

Gene Name

sperm associated antigen 17

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_206996.2		Intron			NP_996879.1
XM_006710426.3		Intron			XP_006710489.1
XM_006710427.3		Intron			XP_006710490.1
XM_006710428.3		Intron			XP_006710491.1
XM_006710429.3		Intron			XP_006710492.1
XM_006710431.3		Intron			XP_006710494.1
XM_011540934.1		Intron			XP_011539236.1
XM_011540935.2		Intron			XP_011539237.1
XM_011540936.2		Intron			XP_011539238.1
XM_011540937.2		Intron			XP_011539239.1
XM_011540939.2		Intron			XP_011539241.1
XM_011540941.2		Intron			XP_011539243.1
XM_011540942.2		Intron			XP_011539244.1

Gene

WDR3

Gene Name

WD repeat domain 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_006784.2		Intron			NP_006775.1

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