Product Details

SNP ID

rs4500055

Assay Type

Validated

NCBI dbSNP Submissions

NA

Location

Chr.8:94824584 on Build GRCh38

Set Membership

HapMap Validated

Context Sequence [VIC/FAM]

CTAATTGGCAGTGGTTATTTGCAGA[A/T]CCAGAAATCTATGACTGTTATGTTC

Phenotype

MIM: 611351

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

INTS8 PubMed Links

Gene Details

Gene

INTS8

Gene Name

integrator complex subunit 8

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_017864.3		Intron			NP_060334.2
XM_017013616.1		Intron			XP_016869105.1
XM_017013617.1		Intron			XP_016869106.1
XM_017013618.1		Intron			XP_016869107.1
XM_017013619.1		Intron			XP_016869108.1

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