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SNP ID

rs141463019

Assay Type

Functionally tested

NCBI dbSNP Submissions

19

Location

Chr.1:231019936 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CAGTGACAAGTCCCGAGGAGGGCCT[C/T]GGTCCCTCCTGTCGTGCAGGGAGTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM89A PubMed Links

Gene Details

Gene

FAM89A

Gene Name

family with sequence similarity 89 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_198552.2	520	Missense Mutation			NP_940954.1

Gene

MIR1182

Gene Name

microRNA 1182

There are no transcripts associated with this gene.

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