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CCGGTTTCATGGAGTCTCCAAGAAC[C/T]GCTAAAGGAGGAAGGGGTAAAGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 607394 | ||||||||||||||||||||
Literature Links: |
OAF 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 |
OAF - out at first homolog | ||||||
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There are no transcripts associated with this gene. |
POU2F3 - POU class 2 homeobox 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001244682.1 | 52 | Silent Mutation | ACC,ACT | T,T 6 | NP_001231611.1 | |
NM_014352.3 | 52 | Intron | NP_055167.2 | |||
XM_011542739.2 | 52 | Intron | XP_011541041.1 | |||
XM_011542740.2 | 52 | Intron | XP_011541042.1 | |||
XM_011542741.2 | 52 | Intron | XP_011541043.1 | |||
XM_011542742.2 | 52 | Intron | XP_011541044.1 | |||
XM_011542743.2 | 52 | Intron | XP_011541045.1 | |||
XM_017017487.1 | 52 | Intron | XP_016872976.1 |