Product Details

SNP ID

rs138534021

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.9:131260991 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGCGATGGGCTCCCGCAGCCGGGCG[C/T]GCTGGCCCAGGGGCCGGTTGGGGTT

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	1023	Missense Mutation	CAC,CGC	H228R	NP_203745.2
XM_011518567.1	1023	Missense Mutation	CAC,CGC	H179R	XP_011516869.1
XM_011518568.2	1023	Missense Mutation	CAC,CGC	H145R	XP_011516870.1

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