Product Details

SNP ID

rs200849898

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:81990861 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

ACTGTTATGCCCAGACCCCGTCTGT[C/T]GGGTGTGTAAGAGAGCAACTGCTGA

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

SPATA31D1 PubMed Links

Gene Details

Gene

SPATA31D1

Gene Name

SPATA31 subfamily D member 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001001670.2	416	Missense Mutation	CGG,TGG	R131W	NP_001001670.1
XM_017014710.1	416	Missense Mutation	CGG,TGG	R94W	XP_016870199.1

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