Product Details

SNP ID
rs111939293
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:94825057 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ACATTTGAAGTGGGACTTAGACATA[C/T]TAGAGAAAAGGTATCCAAGATTTCA
Phenotype
MIM: 611351
Polymorphism
C/T, Transition 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_017864.3 437 Silent Mutation CTA,TTA L99L NP_060334.2
XM_017013616.1 437 Silent Mutation CTA,TTA L99L XP_016869105.1
XM_017013617.1 437 Silent Mutation CTA,TTA L99L XP_016869106.1
XM_017013618.1 437 Intron XP_016869107.1
XM_017013619.1 437 UTR 5 XP_016869108.1

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