Product Details

SNP ID

rs10981763

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:113354346 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AAGAATCAAAGAGCAGTGGTAATTC[C/G]TCTTCTTTCCTCTCTACTCAGCCCC

Phenotype

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

BSPRY PubMed Links

Gene Details

Gene

BSPRY

Gene Name

B-box and SPRY domain containing

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317943.1		Intron			NP_001304872.1
NM_001317944.1		Intron			NP_001304873.1
NM_017688.2		Intron			NP_060158.2
XM_006717149.3		Intron			XP_006717212.1

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