Product Details

SNP ID

rs148621394

Assay Type

Functionally tested

NCBI dbSNP Submissions

14

Location

Chr.1:231020038 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTAAGTGCAGTCTGGGCTGGAGGCT[C/G]CCTGGCATGCCCCCTTGTACTCCTG

Phenotype

Polymorphism

C/G, Transversion 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	418	Missense Mutation	GCA,GGA	A127G	NP_940954.1

Gene

MIR1182

Gene Name

microRNA 1182

There are no transcripts associated with this gene.

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