Product Details

SNP ID
rs8126600
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:42509742 on Build GRCh38
Set Membership
HapMap
Context Sequence [VIC/FAM]
CTTCCTCGCCAGTCAGTGCACCATA[A/C]CATTAGAATTCTTGCTTTTTGATCA
Phenotype
MIM: 608094
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC37A1 PubMed Links

Gene Details

Gene
SLC37A1
Gene Name
solute carrier family 37 member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001320537.1 Intron NP_001307466.1
NM_018964.3 Intron NP_061837.3
XM_011529614.2 Intron XP_011527916.1
XM_011529615.1 Intron XP_011527917.1
XM_017028376.1 Intron XP_016883865.1
XM_017028377.1 Intron XP_016883866.1
XM_017028378.1 Intron XP_016883867.1
XM_017028379.1 Intron XP_016883868.1
XM_017028380.1 Intron XP_016883869.1
XM_017028381.1 Intron XP_016883870.1
XM_017028382.1 Intron XP_016883871.1
XM_017028383.1 Intron XP_016883872.1

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