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CTGGATCATTGGATTGGAACAGCAG[C/T]ACTATTAATCTGAAAAATGGTCAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300654 MIM: 300517 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FAAH2 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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FAAH2 - fatty acid amide hydrolase 2 | ||||||
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There are no transcripts associated with this gene. |
SPIN2B - spindlin family member 2B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001006681.1 | Intron | NP_001006682.1 | ||||
NM_001006682.1 | Intron | NP_001006683.1 | ||||
NM_001006683.1 | Intron | NP_001006684.1 | ||||
NM_001282461.1 | Intron | NP_001269390.1 | ||||
NM_001282462.1 | Intron | NP_001269391.1 | ||||
XM_005262008.4 | Intron | XP_005262065.2 | ||||
XM_005262009.4 | Intron | XP_005262066.2 | ||||
XM_005262010.1 | Intron | XP_005262067.1 | ||||
XM_011530788.2 | Intron | XP_011529090.1 | ||||
XM_011530789.2 | Intron | XP_011529091.1 | ||||
XM_017029552.1 | Intron | XP_016885041.1 |