Product Details

SNP ID
rs61995938
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:47410149 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CATGGCGGGCCCAAGGCTCCTCTTC[C/T]TCACTGCCCTTGCCCTGGAGCTCTT
Phenotype
MIM: 186852 MIM: 608735
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MIR4487 PubMed Links

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_001128225.2 110 Missense Mutation CTC,TTC L19F NP_001121697.1
NM_152264.4 110 Missense Mutation CTC,TTC L19F NP_689477.2
XM_006718381.3 110 Missense Mutation CTC,TTC L34F XP_006718444.1
XM_006718383.3 110 Missense Mutation CTC,TTC L34F XP_006718446.1
XM_006718384.2 110 Missense Mutation CTC,TTC L34F XP_006718447.1
XM_006718385.2 110 Missense Mutation CTC,TTC L34F XP_006718448.1
XM_011520466.1 110 Missense Mutation CTC,TTC L34F XP_011518768.1
XM_011520467.1 110 Missense Mutation CTC,TTC L19F XP_011518769.1
XM_011520468.2 110 Missense Mutation CTC,TTC L19F XP_011518770.1
XM_011520469.1 110 Missense Mutation CTC,TTC L34F XP_011518771.1
XM_011520470.1 110 Missense Mutation CTC,TTC L19F XP_011518772.1
XM_017018540.1 110 Missense Mutation CTC,TTC L19F XP_016874029.1
XM_017018541.1 110 Missense Mutation CTC,TTC L19F XP_016874030.1
XM_017018542.1 110 Missense Mutation CTC,TTC L19F XP_016874031.1

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