Product Details

SNP ID

rs143378086

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:131260985 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCCTGGGCGATGGGCTCCCGCAGC[C/T]GGGCGCGCTGGCCCAGGGGCCGGTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM78A PubMed Links

Gene Details

Gene

FAM78A

Gene Name

family with sequence similarity 78 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_033387.3	1029	Missense Mutation	CAG,CGG	Q230R	NP_203745.2
XM_011518567.1	1029	Missense Mutation	CAG,CGG	Q181R	XP_011516869.1
XM_011518568.2	1029	Missense Mutation	CAG,CGG	Q147R	XP_011516870.1

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