Product Details

SNP ID

rs28756143

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.15:74904241 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TAAGCACAGACTAGCAAACACTTAG[C/G]TGGGATCTATCAAAAGGGTTCCTTT

Phenotype

MIM: 154550

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

FAM219B PubMed Links

Additional Information

For this assay, SNP(s) [rs77509195] are located under a probe 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

FAM219B

Gene Name

family with sequence similarity 219 member B

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001321920.1		Intron			NP_001308849.1
NM_001321921.1		Intron			NP_001308850.1
NM_001321922.1		Intron			NP_001308851.1
NM_001321923.1		Intron			NP_001308852.1
NM_020447.4		Intron			NP_065180.1
XM_017022433.1		Intron			XP_016877922.1

Gene

MPI

Gene Name

mannose phosphate isomerase

There are no transcripts associated with this gene.

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