Product Details

SNP ID
rs17854443
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.11:93148767 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATTTCAACCAAAGGTGGCAGGATTA[G/T]GGCCAATGTGCTGCTGCTCACAGCT
Phenotype
MIM: 613760
Polymorphism
G/T, Transversion Substitution
Allele Nomenclature
Literature Links
SLC36A4 PubMed Links

Gene Details

Gene
SLC36A4
Gene Name
solute carrier family 36 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001286139.1 1428 Missense Mutation ATA,CTA I294L NP_001273068.1
NM_152313.3 1428 Missense Mutation ATA,CTA I429L NP_689526.2
XM_017017174.1 1428 UTR 3 XP_016872663.1
XM_017017175.1 1428 Missense Mutation ATA,CTA I323L XP_016872664.1
XM_017017176.1 1428 Missense Mutation ATA,CTA I294L XP_016872665.1
XM_017017177.1 1428 UTR 3 XP_016872666.1

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