Product Details

SNP ID
rs34088699
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.6:8416378 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCTCCAAAGCAGAACAAATACAACT[C/G]ATTTTTCTACAGGGCCAAGCAAAGA
Phenotype
MIM: 610845
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
SLC35B3 PubMed Links

Gene Details

Gene
SLC35B3
Gene Name
solute carrier family 35 member B3
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001142541.2 Intron NP_001136013.1
NM_015948.4 Intron NP_057032.2
XM_005249156.3 Intron XP_005249213.1
XM_005249157.2 Intron XP_005249214.1
XM_005249158.1 Intron XP_005249215.1
XM_006715102.3 Intron XP_006715165.1
XM_006715103.3 Intron XP_006715166.1
XM_011514648.1 Intron XP_011512950.1
XM_011514650.2 Intron XP_011512952.1
XM_017010910.1 Intron XP_016866399.1
XM_017010911.1 Intron XP_016866400.1
XM_017010912.1 Intron XP_016866401.1
XM_017010913.1 Intron XP_016866402.1
XM_017010914.1 Intron XP_016866403.1
XM_017010915.1 Intron XP_016866404.1

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