Product Details

SNP ID

rs10172787

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:121764240 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

GTAGGCTGTACCACTTGTCTGGCTT[C/G]TTGGAGACACCTGACCAGTAAACAG

Phenotype

MIM: 600575

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

TSN PubMed Links

Gene Details

Gene

TSN

Gene Name

translin

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001261401.1		Intron			NP_001248330.1
NM_004622.2		Intron			NP_004613.1

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