Product Details

SNP ID

rs144431781

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:126556588 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCGGGTGCAGGTGCGTGGCGAGCT[C/T]CTGCAGCACGGCCGCGCGCCCGATC

Phenotype

MIM: 609483

Polymorphism

C/T, Transition 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	1331	Missense Mutation			NP_777571.1
XM_017013107.1	1331	Missense Mutation			XP_016868596.1
XM_017013108.1	1331	Missense Mutation			XP_016868597.1

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