Product Details

SNP ID
rs1062724
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:68006702 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGTGCAATGCTACTCTGCCATGGA[G/T]CCCTTCAGCACACTTTCCAGCAGCA
Phenotype
Polymorphism
G/T, Transversion substitution
Allele Nomenclature
Literature Links
FAM19A1 PubMed Links

Gene Details

Gene
FAM19A1
Gene Name
family with sequence similarity 19 member A1, C-C motif chemokine like
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001252216.1 1209 Missense Mutation GCC,TCC A26S NP_001239145.1
NM_213609.3 1209 Missense Mutation GCC,TCC A26S NP_998774.2
XM_017006386.1 1209 Missense Mutation GCC,TCC A26S XP_016861875.1
XM_017006387.1 1209 Missense Mutation GCC,TCC A26S XP_016861876.1
XM_017006388.1 1209 Missense Mutation GCC,TCC A26S XP_016861877.1
XM_017006389.1 1209 Missense Mutation GCC,TCC A26S XP_016861878.1
XM_017006390.1 1209 Missense Mutation GCC,TCC A26S XP_016861879.1

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