Product Details

SNP ID

rs35212289

Assay Type

Functionally tested

NCBI dbSNP Submissions

12

Location

Chr.1:153776586 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CATGGGGCTCCACCTGTGGGCTGCA[C/G]GCCCAGGAACCCACCCTGCTGGAAT

Phenotype

MIM: 611347 MIM: 604193

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

INTS3 PubMed Links

Gene Details

Gene

INTS3

Gene Name

integrator complex subunit 3

There are no transcripts associated with this gene.

Gene

SLC27A3

Gene Name

solute carrier family 27 member 3

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317929.1	942	Missense Mutation	CGC,GGC	R293G	NP_001304858.1
NM_024330.1	942	Missense Mutation	CGC,GGC	R293G	NP_077306.1

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