Product Details

SNP ID

rs8128752

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.21:14487231 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TTCATCCCATTCCAGTGAGAATAAA[A/G]TAAATCCAAACCTCAGAATCCTTCA

Phenotype

MIM: 607978

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

SAMSN1 PubMed Links

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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