Product Details

SNP ID

rs76698360

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.12:12975340 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TTCAACAGCCAGATCTCATTGCGCC[A/G]TCCGTAGGGCTTCATGGGAGGGTCA

Phenotype

MIM: 605826

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

FAM234B PubMed Links

Additional Information

For this assay, SNP(s) [rs1941] are located under a primer sequence. To help evaluate the possible impact of a given SNP on your experiment, please refer to the 1000 Genomes and NCBI dbSNP databases. A higher minor allele frequency in your study population represents a higher risk to assay performance.

Gene Details

Gene

FAM234B

Gene Name

family with sequence similarity 234 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020853.1	733	Intron			NP_065904.1
XM_017019706.1	733	Intron			XP_016875195.1

Gene

HEBP1

Gene Name

heme binding protein 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_015987.4	733	Missense Mutation	CGG,TGG	R180W	NP_057071.2

Gene

LOC100506314

Gene Name

uncharacterized LOC100506314

There are no transcripts associated with this gene.

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