Product Details

SNP ID
rs149216450
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.5:69104649 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTTATAGTGGATCAAAATATTTAAA[C/T]ATGCAGTTGCTGGGTGTATTATTTC
Phenotype
MIM: 607819
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
SLC30A5 PubMed Links

Gene Details

Gene
SLC30A5
Gene Name
solute carrier family 30 member 5
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001251969.1 429 UTR 3 NP_001238898.1
NM_022902.4 429 Missense Mutation CAT,TAT H98Y NP_075053.2
NM_024055.4 429 UTR 3 NP_076960.1
XM_005248569.3 429 Missense Mutation CAT,TAT H57Y XP_005248626.1
XM_006714672.3 429 Missense Mutation CAT,TAT H98Y XP_006714735.1
XM_017009749.1 429 Missense Mutation CAT,TAT H57Y XP_016865238.1

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