Product Details

SNP ID

rs148176598

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:126556612 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTGCAGCACGGCCGCGCGCCCGA[A/T]CTGGTCGTTGCGTCGCTTCTCCATG

Phenotype

MIM: 609483

Polymorphism

A/T, Transversion substitution

Allele Nomenclature

Literature Links

FAM84B PubMed Links

Gene Details

Gene

FAM84B

Gene Name

family with sequence similarity 84 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_174911.4	1307	Missense Mutation	ATC,TTC	I260F	NP_777571.1
XM_017013107.1	1307	Missense Mutation	ATC,TTC	I260F	XP_016868596.1
XM_017013108.1	1307	Missense Mutation	ATC,TTC	I242F	XP_016868597.1

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