Product Details

SNP ID

rs138420595

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.22:35067106 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCCCTCAATGTGTGCTGAGGTGGGC[A/C]CTGCTCTCTGCAGGGGTATGGAGAG

Phenotype

MIM: 612019

Polymorphism

A/C, Transversion substitution

Allele Nomenclature

Literature Links

ISX PubMed Links

Gene Details

Gene

ISX

Gene Name

intestine specific homeobox

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001303508.1	682	Missense Mutation	ACT,CCT	T7P	NP_001290437.1

View Full Product Details