Product Details

SNP ID
rs201360580
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.14:57564216 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGCTGGGATCAGTCACATCATCCAC[A/G]TGCTCCTCACTCTTCTTTTCCTTCA
Phenotype
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
SLC35F4 PubMed Links

Gene Details

Gene
SLC35F4
Gene Name
solute carrier family 35 member F4
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001206920.1 1691 Silent Mutation CAC,CAT H458H NP_001193849.1
NM_001306087.1 1691 Silent Mutation CAC,CAT H459H NP_001293016.1
XM_011536720.2 1691 Silent Mutation CAC,CAT H506H XP_011535022.1
XM_011536721.2 1691 Silent Mutation CAC,CAT H505H XP_011535023.1
XM_011536723.2 1691 Silent Mutation CAC,CAT H446H XP_011535025.1
XM_011536724.2 1691 Silent Mutation CAC,CAT H441H XP_011535026.1
XM_011536725.1 1691 Silent Mutation CAC,CAT H336H XP_011535027.1
XM_017021258.1 1691 Silent Mutation CAC,CAT H506H XP_016876747.1
XM_017021259.1 1691 Intron XP_016876748.1
XM_017021260.1 1691 Silent Mutation CAC,CAT H336H XP_016876749.1
XM_017021261.1 1691 Intron XP_016876750.1

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