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AGACAATGGAAAAGTTGTTAATTAT[A/G]CAAGGAAAAATGGTGACTTGTACAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 610491 | ||||||||||||||||||||
Literature Links: |
MIR3665 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
MIR3665 - microRNA 3665 | ||||||
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There are no transcripts associated with this gene. |
SLAIN1 - SLAIN motif family member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | 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 |