Product Details

SNP ID

rs9983264

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.21:14489319 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCAGTGCATCTTTTTATACTAAAAC[A/G]TTTCTGATAATACGCTAGGTTTAAA

Phenotype

MIM: 607978

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

SAMSN1 PubMed Links

Additional Information

For this assay, SNP(s) [rs117825494] are located under a probe sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

SAMSN1

Gene Name

SAM domain, SH3 domain and nuclear localization signals 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256370.1		Intron			NP_001243299.1
NM_001286523.1		Intron			NP_001273452.1
NM_022136.4		Intron			NP_071419.3
XM_011529684.2		Intron			XP_011527986.1
XM_011529685.1		Intron			XP_011527987.1
XM_011529686.1		Intron			XP_011527988.1
XM_017028427.1		Intron			XP_016883916.1

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