Product Details

SNP ID

rs150046345

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:153776089 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCCGGCCTGCGCACTGCCTTTGTG[C/T]CCACCGCCCTGCGCCGGGGCCCCCT

Phenotype

MIM: 611347 MIM: 604193

Polymorphism

C/T, Transition 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	798	Missense Mutation	CCC,TCC	P245S	NP_001304858.1
NM_024330.1	798	Missense Mutation	CCC,TCC	P245S	NP_077306.1

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