Product Details

SNP ID: rs187893622
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.3:68006683 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: TGTATTTGTGGATAAGTGCTTGTGC[A/G]ATGCTACTCTGCCATGGATCCCTTC
Phenotype
Polymorphism: A/G, Transition 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	1190	Silent Mutation	GCA,GCG	A19A	NP_001239145.1
NM_213609.3	1190	Silent Mutation	GCA,GCG	A19A	NP_998774.2
XM_017006386.1	1190	Silent Mutation	GCA,GCG	A19A	XP_016861875.1
XM_017006387.1	1190	Silent Mutation	GCA,GCG	A19A	XP_016861876.1
XM_017006388.1	1190	Silent Mutation	GCA,GCG	A19A	XP_016861877.1
XM_017006389.1	1190	Silent Mutation	GCA,GCG	A19A	XP_016861878.1
XM_017006390.1	1190	Silent Mutation	GCA,GCG	A19A	XP_016861879.1