Product Details

SNP ID

rs1681072

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:55902181 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TGCTCAAGGCCTCTGCCTCTCCTTT[A/C]TCTTGCTGCTGCCGCCTCTTCTCCT

Phenotype

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

PYM1 PubMed Links

Gene Details

Gene

PYM1

Gene Name

PYM homolog 1, exon junction complex associated factor

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143853.1	458	Silent Mutation			NP_001137325.1
NM_032345.2	458	Silent Mutation			NP_115721.1

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