Product Details

SNP ID
rs13418
Assay Type
Functionally tested
NCBI dbSNP Submissions
1
Location
Chr.1:211942063 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AATTGAGTACTGAAGTAATCATTAT[G/T]AGGTTCAACCCTTTGCTCCATCTCA
Phenotype
MIM: 611350
Polymorphism
G/T, Transversion 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 2831 Missense Mutation AAT,CAT N835H NP_001186738.1
NM_001199811.1 2831 Missense Mutation AAT,CAT N870H NP_001186740.1
NM_001199812.1 2831 Missense Mutation AAT,CAT N864H NP_001186741.1
NM_015434.3 2831 Missense Mutation AAT,CAT N884H NP_056249.1
XM_011509396.2 2831 Missense Mutation AAT,CAT N920H XP_011507698.1
XM_017000962.1 2831 Intron XP_016856451.1

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