Product Details

SNP ID

rs149689841

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.19:19120062 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GGGGAGTAAGCAGGCCACCCAGAGC[C/G]CCGGCAATCCGCGCTGCAGTCTGCT

Phenotype

MIM: 610823

Polymorphism

C/G, Transversion Substitution

Allele Nomenclature

Literature Links

SLC25A42 PubMed Links

Additional Information

For this assay, SNP(s) [rs756791] 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

SLC25A42

Gene Name

solute carrier family 25 member 42

There are no transcripts associated with this gene.

Gene

TMEM161A

Gene Name

transmembrane protein 161A

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001256766.1	1277	Silent Mutation	GGC,GGG	G333G	NP_001243695.1
NM_017814.2	1277	Silent Mutation	GGC,GGG	G436G	NP_060284.1
XM_011528117.2	1277	Silent Mutation	GGC,GGG	G234G	XP_011526419.1
XM_017026916.1	1277	Silent Mutation	GGC,GGG	G411G	XP_016882405.1

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