Product Details

SNP ID

rs113067579

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.14:58407900 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCTTGGTGTATGTATGCATCAACT[A/G]GAATTTCCTGCAAATGCTTGGATTC

Phenotype

MIM: 607384

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

TIMM9 PubMed Links

Additional Information

For this assay, SNP(s) [rs200959055] 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

TIMM9

Gene Name

translocase of inner mitochondrial membrane 9

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001304485.1		Intron			NP_001291414.1
NM_001304486.1		Intron			NP_001291415.1
NM_001304487.1		Intron			NP_001291416.1
NM_001304488.1		Intron			NP_001291417.1
NM_001304489.1		Intron			NP_001291418.1
NM_001304490.1		Intron			NP_001291419.1
NM_001304491.1		Intron			NP_001291420.1
NM_012460.3		Intron			NP_036592.1

Gene

TOMM20L

Gene Name

translocase of outer mitochondrial membrane 20 like

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_207377.2		Intron			NP_997260.1
XM_011536742.2		Intron			XP_011535044.1
XM_011536743.2		Intron			XP_011535045.1
XM_011536744.2		Intron			XP_011535046.1

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