Product Details

SNP ID
rs149531895
Assay Type
Functionally tested
NCBI dbSNP Submissions
4
Location
Chr.1:211942081 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCATTATGAGGTTCAACCCTTTGCT[C/G]CATCTCATTGGTCATGTTGTCAATG
Phenotype
MIM: 611350
Polymorphism
C/G, 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 2813 Missense Mutation CAG,GAG Q829E NP_001186738.1
NM_001199811.1 2813 Missense Mutation CAG,GAG Q864E NP_001186740.1
NM_001199812.1 2813 Missense Mutation CAG,GAG Q858E NP_001186741.1
NM_015434.3 2813 Missense Mutation CAG,GAG Q878E NP_056249.1
XM_011509396.2 2813 Missense Mutation CAG,GAG Q914E XP_011507698.1
XM_017000962.1 2813 Intron XP_016856451.1

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