Product Details

SNP ID
rs12874992
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:77701298 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TGTAGATTAATCACTGGATATTTTA[C/G]CTATTCTTTTATGTAAGTATATCTT
Phenotype
MIM: 610491
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
MIR3665 PubMed Links

Gene Details

Gene
MIR3665
Gene Name
microRNA 3665
There are no transcripts associated with this gene.

Gene
SLAIN1
Gene Name
SLAIN motif family member 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001040153.3 Intron NP_001035243.2
NM_001242868.1 Intron NP_001229797.1
NM_001242869.1 Intron NP_001229798.1
NM_001242870.1 Intron NP_001229799.1
NM_001242871.1 Intron NP_001229800.1
NM_144595.3 Intron NP_653196.1
XM_011534929.2 Intron XP_011533231.1
XM_011534930.1 Intron XP_011533232.1

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