Product Details

SNP ID
rs2688
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.17:37686928 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
TCTTTAAAAGAAATCTCAAGATCAT[G/T]TGGGATGGGGGCAGGGGAGGGAGTC
Phenotype
MIM: 189907
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
HNF1B PubMed Links

Gene Details

Gene
HNF1B
Gene Name
HNF1 homeobox B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000458.3 2096 UTR 3 NP_000449.1
NM_001165923.3 2096 UTR 3 NP_001159395.1
NM_001304286.1 2096 UTR 3 NP_001291215.1
XM_011525160.1 2096 UTR 3 XP_011523462.1
XM_011525161.1 2096 UTR 3 XP_011523463.1
XM_011525162.2 2096 Intron XP_011523464.1
XM_011525163.2 2096 Intron XP_011523465.1
XM_011525164.1 2096 UTR 3 XP_011523466.1

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