Product Details

SNP ID

rs143716190

Assay Type

Functionally tested

NCBI dbSNP Submissions

8

Location

Chr.1:117957146 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTAAACTCTTTAACGAATTCATTCA[A/G]CTGGGCTCTGATGTTGAACTTATAT

Phenotype

MIM: 616554 MIM: 604737

Polymorphism

A/G, 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	2598	Intron			NP_996879.1
XM_006710426.3	2598	Intron			XP_006710489.1
XM_006710427.3	2598	Intron			XP_006710490.1
XM_006710428.3	2598	Intron			XP_006710491.1
XM_006710429.3	2598	Intron			XP_006710492.1
XM_006710431.3	2598	Intron			XP_006710494.1
XM_011540934.1	2598	Intron			XP_011539236.1
XM_011540935.2	2598	Intron			XP_011539237.1
XM_011540936.2	2598	Intron			XP_011539238.1
XM_011540937.2	2598	Intron			XP_011539239.1
XM_011540939.2	2598	Intron			XP_011539241.1
XM_011540941.2	2598	Intron			XP_011539243.1
XM_011540942.2	2598	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	2598	Silent Mutation	CAA,CAG	Q844Q	NP_006775.1

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