Product Details

SNP ID

rs147355005

Assay Type

Functionally tested

NCBI dbSNP Submissions

7

Location

Chr.1:117959342 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTTGATTATCTCAAGAGGGAATG[C/T]GAGGCAAAAAGTGAAGTTATGTTTT

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	2793	Intron			NP_996879.1
XM_006710426.3	2793	Intron			XP_006710489.1
XM_006710427.3	2793	Intron			XP_006710490.1
XM_006710428.3	2793	Intron			XP_006710491.1
XM_006710429.3	2793	Intron			XP_006710492.1
XM_006710431.3	2793	Intron			XP_006710494.1
XM_011540934.1	2793	Intron			XP_011539236.1
XM_011540935.2	2793	Intron			XP_011539237.1
XM_011540936.2	2793	Intron			XP_011539238.1
XM_011540937.2	2793	Intron			XP_011539239.1
XM_011540939.2	2793	Intron			XP_011539241.1
XM_011540941.2	2793	Intron			XP_011539243.1
XM_011540942.2	2793	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	2793	Silent Mutation	TGC,TGT	C909C	NP_006775.1

View Full Product Details