Product Details

SNP ID
rs117712299
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.9:96313822 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTCTGGTCTTGTCAGATCATCTCTC[A/C]CCAGTGTGGAACAGCCTTCCAAGTG
Phenotype
MIM: 605573 MIM: 609182
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
HSD17B3 PubMed Links

Gene Details

Gene
HSD17B3
Gene Name
hydroxysteroid 17-beta dehydrogenase 3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_000197.1 Intron NP_000188.1
XM_011518618.2 Intron XP_011516920.1
XM_011518619.2 Intron XP_011516921.1
XM_017014671.1 Intron XP_016870160.1
XM_017014672.1 Intron XP_016870161.1
XM_017014673.1 Intron XP_016870162.1
XM_017014674.1 Intron XP_016870163.1
XM_017014675.1 Intron XP_016870164.1
XM_017014676.1 Intron XP_016870165.1
XM_017014677.1 Intron XP_016870166.1
Gene
SLC35D2
Gene Name
solute carrier family 35 member D2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286990.1 Intron NP_001273919.1
NM_007001.2 Intron NP_008932.2
XM_005251673.1 Intron XP_005251730.1
XM_005251674.1 Intron XP_005251731.1
XM_005251675.2 Intron XP_005251732.1
XM_005251676.1 Intron XP_005251733.1
XM_005251678.4 Intron XP_005251735.1
XM_006716939.2 Intron XP_006717002.1
XM_011518164.1 Intron XP_011516466.1

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