Product Details

SNP ID

rs200016935

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:123775281 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CTTGAGGATAACACCATTTTCATAT[C/T]ATACTGGGATTATGGAGGTGAGTTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM91A1 PubMed Links

Gene Details

Gene

FAM91A1

Gene Name

family with sequence similarity 91 member A1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001317917.1	556	UTR 5			NP_001304846.1
NM_001317918.1	556	Missense Mutation	CAT,TAT	H98Y	NP_001304847.1
NM_144963.3	556	Missense Mutation	CAT,TAT	H98Y	NP_659400.2

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