Product Details

SNP ID
rs12349592
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:36143929 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TTCCCCTCTGGGGCCCCAGAATTCA[A/T]CAGAGGCCTCCACCGTGTCTTCCAG
Phenotype
MIM: 607141
Polymorphism
A/T, Transversion substitution
Allele Nomenclature
Literature Links
GLIPR2 PubMed Links

Gene Details

Gene
GLIPR2
Gene Name
GLI pathogenesis related 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001287010.1 Intron NP_001273939.1
NM_001287011.1 Intron NP_001273940.1
NM_001287012.1 Intron NP_001273941.1
NM_001287013.1 Intron NP_001273942.1
NM_001287014.1 Intron NP_001273943.1
NM_022343.3 Intron NP_071738.1

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