Product Details

SNP ID
rs2788139
Assay Type
Functionally tested
NCBI dbSNP Submissions
56
Location
Chr.1:211940653 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CAACCAGAATTAAAATAGGAAAAAA[A/G]GGGGTTTTCTGGCTAACCAGAAAAC
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 4241 UTR 3 NP_001186738.1
NM_001199811.1 4241 UTR 3 NP_001186740.1
NM_001199812.1 4241 UTR 3 NP_001186741.1
NM_015434.3 4241 UTR 3 NP_056249.1
XM_011509396.2 4241 UTR 3 XP_011507698.1
XM_017000962.1 4241 Intron XP_016856451.1

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