Product Details

SNP ID
rs200641765
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:155298617 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACCTGCTGCAGATCCAGAGGAATG[C/T]CACTCTCTTCCCCGAGGAGGTGATC
Phenotype
MIM: 602055
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
INSIG1 PubMed Links

Gene Details

Gene
INSIG1
Gene Name
insulin induced gene 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005542.4 543 Missense Mutation GCC,GTC A111V NP_005533.2
NM_198336.2 543 Intron NP_938150.2
NM_198337.2 543 Missense Mutation GCC,GTC A111V NP_938151.1
XM_005249542.1 543 Missense Mutation GCC,GTC A111V XP_005249599.1
XM_005249543.1 543 Missense Mutation GCC,GTC A111V XP_005249600.1
XM_017012177.1 543 Missense Mutation GCC,GTC A111V XP_016867666.1

View Full Product Details