Product Details

SNP ID

rs201972895

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.17:44320682 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

CCACAGAAGTCTGGTCCTTCGGCCT[A/G]AACCCATTGAGCCAGCTCTTCACCA

Phenotype

MIM: 605448 MIM: 610820

Polymorphism

A/G, Transition Substitution

Allele Nomenclature

Literature Links

RUNDC3A PubMed Links

Additional Information

For this assay, SNP(s) [rs2011951] 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

RUNDC3A

Gene Name

RUN domain containing 3A

There are no transcripts associated with this gene.

Gene

SLC25A39

Gene Name

solute carrier family 25 member 39

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001143780.2	831	Silent Mutation			NP_001137252.1
NM_001321240.1	831	Silent Mutation			NP_001308169.1
NM_001321241.1	831	Silent Mutation			NP_001308170.1
NM_016016.3	831	Silent Mutation			NP_057100.1
XM_011524880.2	831	Silent Mutation			XP_011523182.1
XM_011524882.2	831	Silent Mutation			XP_011523184.1
XM_011524883.2	831	Silent Mutation			XP_011523185.1
XM_011524884.1	831	Silent Mutation			XP_011523186.1
XM_017024737.1	831	Silent Mutation			XP_016880226.1

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