Product Details

SNP ID

rs2788137

Assay Type

Functionally tested

NCBI dbSNP Submissions

32

Location

Chr.1:211943260 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

CTGCAAAGTAATCATGTTATTACTC[A/G]GCTTATTATATCAGCTTCCTGACTT

Phenotype

MIM: 611350

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

INTS7 PubMed Links

Gene Details

Gene

INTS7

Gene Name

integrator complex subunit 7

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001199809.1		Intron			NP_001186738.1
NM_001199811.1		Intron			NP_001186740.1
NM_001199812.1		Intron			NP_001186741.1
NM_015434.3		Intron			NP_056249.1
XM_011509396.2		Intron			XP_011507698.1
XM_017000962.1		Intron			XP_016856451.1

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