Product Details

SNP ID
rs147679713
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.10:15213160 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCAACAAGCATCGCAGGGCACTGT[C/T]CTCGGGGGTACAGACCGTGGTCCCA
Phenotype
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
FAM171A1 PubMed Links

Gene Details

Gene
FAM171A1
Gene Name
family with sequence similarity 171 member A1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001010924.1 2356 Missense Mutation AAC,GAC N810D NP_001010924.1
XM_011519378.2 2356 Missense Mutation AAC,GAC N797D XP_011517680.1
XM_017015904.1 2356 Missense Mutation AAC,GAC N781D XP_016871393.1
XM_017015905.1 2356 Missense Mutation AAC,GAC N452D XP_016871394.1

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