Product Details

SNP ID

rs146253684

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.14:35046540 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCTGTGGTGGCGACGACGATGGACC[A/G]GGAGCCAGTGGGCGGTGTGGAACGA

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

FAM177A1 PubMed Links

Gene Details

Gene

FAM177A1

Gene Name

family with sequence similarity 177 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001079519.1	467	Missense Mutation	CAG,CGG	Q3R	NP_001072987.1
NM_001289022.1	467	Missense Mutation	CAG,CGG	Q3R	NP_001275951.1
NM_173607.3	467	Missense Mutation	CAG,CGG	Q26R	NP_775878.2

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