Product Details

SNP ID

rs6580742

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.12:50334028 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

TCCCGTAGTCATCAAGTCTGCTCAG[C/T]ATCATGTGGAGGTTCCTGGCCTCAT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM186A PubMed Links

Gene Details

Gene

FAM186A

Gene Name

family with sequence similarity 186 member A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001145475.1	6728	Missense Mutation	ATA,ATG	I2193M	NP_001138947.1
XM_006719231.3	6728	Missense Mutation	ATA,ATG	I2193M	XP_006719294.1
XM_011537890.2	6728	Missense Mutation	ATA,ATG	I2193M	XP_011536192.1
XM_011537892.1	6728	Missense Mutation	ATA,ATG	I2050M	XP_011536194.1

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