Product Details

SNP ID

rs16895365

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.4:17635043 on Build GRCh38

Set Membership

HapMap

Context Sequence [VIC/FAM]

AGGGGTCAAATATCCCGGGTGAGGA[C/T]TGAAAGAGAAAGACCGATTCCGGTG

Phenotype

MIM: 610311

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FAM184B PubMed Links

Gene Details

Gene

FAM184B

Gene Name

family with sequence similarity 184 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015688.1	3068	Missense Mutation	AAT,AGT	N952S	NP_056503.1

Gene

MED28

Gene Name

mediator complex subunit 28

There are no transcripts associated with this gene.

View Full Product Details