Product Details

SNP ID
rs1129825
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:155298364 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCGCCGAGGCCCCCCGCGAGCCAGC[A/G]CCGCGGGGCTGGCGGCCAAGGTTGG
Phenotype
MIM: 602055
Polymorphism
A/G, 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_005542.4 290 Missense Mutation ACC,GCC T27A NP_005533.2
NM_198336.2 290 Missense Mutation ACC,GCC T27A NP_938150.2
NM_198337.2 290 Missense Mutation ACC,GCC T27A NP_938151.1
XM_005249542.1 290 Missense Mutation ACC,GCC T27A XP_005249599.1
XM_005249543.1 290 Missense Mutation ACC,GCC T27A XP_005249600.1
XM_017012177.1 290 Missense Mutation ACC,GCC T27A XP_016867666.1

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