Product Details

SNP ID

rs143892979

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:158127540 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTTGACTTTCCCAATACACTTTA[C/T]CAAGAAACAGAGACTGAAGAAGTTT

Phenotype

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM198B PubMed Links

Gene Details

Gene

FAM198B

Gene Name

family with sequence similarity 198 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031700.2	1858	Missense Mutation	GAT,GGT	D484G	NP_001026870.2
NM_001128424.1	1858	Missense Mutation	GAT,GGT	D476G	NP_001121896.1
NM_016613.6	1858	Missense Mutation	GAT,GGT	D476G	NP_057697.2

View Full Product Details