Product Details

SNP ID
rs28413169
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:19817496 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCGGCTGAGAGTCCAGAGCCGGAC[A/G]TTCCGGCCGCTTCGGGCTGGCGGCT
Phenotype
MIM: 611353
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
INTS10 PubMed Links

Gene Details

Gene
INTS10
Gene Name
integrator complex subunit 10
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_018142.2 132 UTR 5 NP_060612.2
XM_005273555.3 132 UTR 5 XP_005273612.1
XM_005273556.3 132 UTR 5 XP_005273613.1
XM_005273557.3 132 UTR 5 XP_005273614.1
XM_006716355.2 132 UTR 5 XP_006716418.1
XM_017013606.1 132 UTR 5 XP_016869095.1
XM_017013607.1 132 UTR 5 XP_016869096.1
XM_017013608.1 132 Intron XP_016869097.1
XM_017013609.1 132 UTR 5 XP_016869098.1

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