Product Details

SNP ID

rs140844921

Assay Type

Functionally Tested

NCBI dbSNP Submissions

NA

Location

Chr.11:47410172 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TCCTCACTGCCCTTGCCCTGGAGCT[A/C]TTGGAAAGGGCTGGGGGTTCCCAGC

Phenotype

MIM: 186852 MIM: 608735

Polymorphism

A/C, Transversion Substitution

Allele Nomenclature

Literature Links

MIR4487 PubMed Links

Additional Information

For this assay, SNP(s) [rs2010519] 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

MIR4487

Gene Name

microRNA 4487

There are no transcripts associated with this gene.

Gene

PSMC3

Gene Name

proteasome 26S subunit, ATPase 3

There are no transcripts associated with this gene.

Gene

SLC39A13

Gene Name

solute carrier family 39 member 13

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001128225.2	133	Silent Mutation	CTA,CTC	L26L	NP_001121697.1
NM_152264.4	133	Silent Mutation	CTA,CTC	L26L	NP_689477.2
XM_006718381.3	133	Silent Mutation	CTA,CTC	L41L	XP_006718444.1
XM_006718383.3	133	Silent Mutation	CTA,CTC	L41L	XP_006718446.1
XM_006718384.2	133	Silent Mutation	CTA,CTC	L41L	XP_006718447.1
XM_006718385.2	133	Silent Mutation	CTA,CTC	L41L	XP_006718448.1
XM_011520466.1	133	Silent Mutation	CTA,CTC	L41L	XP_011518768.1
XM_011520467.1	133	Silent Mutation	CTA,CTC	L26L	XP_011518769.1
XM_011520468.2	133	Silent Mutation	CTA,CTC	L26L	XP_011518770.1
XM_011520469.1	133	Silent Mutation	CTA,CTC	L41L	XP_011518771.1
XM_011520470.1	133	Silent Mutation	CTA,CTC	L26L	XP_011518772.1
XM_017018540.1	133	Silent Mutation	CTA,CTC	L26L	XP_016874029.1
XM_017018541.1	133	Silent Mutation	CTA,CTC	L26L	XP_016874030.1
XM_017018542.1	133	Silent Mutation	CTA,CTC	L26L	XP_016874031.1

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