Product Details

SNP ID

rs146876313

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.16:67540096 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCATACTGTGTCCAGCGGCGTCTCC[A/G]GGATGGTGCCTACAACATGGTCCGT

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM65A PubMed Links

Gene Details

Gene

FAM65A

Gene Name

family with sequence similarity 65 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001193522.1	591	Missense Mutation	CAG,CGG	Q157R	NP_001180451.1
NM_001193523.1	591	Missense Mutation	CAG,CGG	Q173R	NP_001180452.1
NM_001193524.1	591	Missense Mutation	CAG,CGG	Q167R	NP_001180453.1
NM_024519.3	591	Missense Mutation	CAG,CGG	Q153R	NP_078795.2
XM_011523321.1	591	Missense Mutation	CAG,CGG	Q173R	XP_011521623.1
XM_011523322.1	591	Missense Mutation	CAG,CGG	Q173R	XP_011521624.1
XM_011523324.2	591	Missense Mutation	CAG,CGG	Q167R	XP_011521626.1
XM_011523325.1	591	Missense Mutation	CAG,CGG	Q153R	XP_011521627.1
XM_011523326.1	591	Missense Mutation	CAG,CGG	Q153R	XP_011521628.1
XM_017023663.1	591	Missense Mutation	CAG,CGG	Q173R	XP_016879152.1
XM_017023664.1	591	UTR 5			XP_016879153.1

View Full Product Details