Product Details

SNP ID
rs41315030
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.13:77698921 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CCCAGTGTTTTCGGAGGGATGACGG[A/G]GGATGGTAGGGGTTGGCCTCTGTCT
Phenotype
MIM: 610491
Polymorphism
A/G, Transition 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_001040153.3 280 UTR 5 NP_001035243.2
NM_001242868.1 280 Intron NP_001229797.1
NM_001242869.1 280 Intron NP_001229798.1
NM_001242870.1 280 Intron NP_001229799.1
NM_001242871.1 280 Intron NP_001229800.1
NM_144595.3 280 Intron NP_653196.1
XM_011534929.2 280 UTR 5 XP_011533231.1
XM_011534930.1 280 Intron XP_011533232.1

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