Product Details

SNP ID
rs17855675
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:5291194 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CACTGGCAGCTGTCCTCCTGAACAA[A/C]GTCCTGGTGGAGAGACTGACCCTGC
Phenotype
MIM: 609149
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
SLC29A4 PubMed Links

Gene Details

Gene
SLC29A4
Gene Name
solute carrier family 29 member 4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040661.1 553 Silent Mutation AAA,AAC K124N NP_001035751.1
NM_001300847.1 553 Silent Mutation AAA,AAC K124N NP_001287776.1
NM_153247.2 553 Silent Mutation AAA,AAC K124N NP_694979.2
XM_005249658.4 553 Missense Mutation AAA,AAC K124N XP_005249715.1
XM_006715667.3 553 Silent Mutation AAA,AAC K124N XP_006715730.1
XM_006715668.2 553 UTR 5 XP_006715731.1
XM_011515200.2 553 Missense Mutation AAA,AAC K124N XP_011513502.1
XM_011515201.2 553 Missense Mutation AAA,AAC K124N XP_011513503.1

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