Product Details

SNP ID

rs495337

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.20:49905793 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

AGGTGTTGGTGGCGCCTGGGCGGTT[A/G]CAGAAGCCACAGCGGGAAGTGGGCG

Phenotype

MIM: 607662

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SPATA2 PubMed Links

Gene Details

Gene

SPATA2

Gene Name

spermatogenesis associated 2

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001135773.1	1612	Silent Mutation	TGC,TGT	C463C	NP_001129245.1
NM_006038.3	1612	Silent Mutation	TGC,TGT	C463C	NP_006029.1
XM_006723894.1	1612	Silent Mutation	TGC,TGT	C463C	XP_006723957.1
XM_011529116.1	1612	Silent Mutation	TGC,TGT	C463C	XP_011527418.1

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