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AAGTAGGTGACCATAGTTTTGATGA[C/T]CCAGGAACTGTAAATGTGCTTGCTT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606586 MIM: 616344 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAI14 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)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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RAI14 - retinoic acid induced 14 | ||||||
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There are no transcripts associated with this gene. |
TTC23L - tetratricopeptide repeat domain 23 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317949.1 | Intron | NP_001304878.1 | ||||
NM_144725.3 | Intron | NP_653326.3 | ||||
XM_011513984.2 | Intron | XP_011512286.1 | ||||
XM_011513985.2 | Intron | XP_011512287.1 | ||||
XM_011513987.2 | Intron | XP_011512289.1 | ||||
XM_017009119.1 | Intron | XP_016864608.1 | ||||
XM_017009120.1 | Intron | XP_016864609.1 | ||||
XM_017009121.1 | Intron | XP_016864610.1 | ||||
XM_017009122.1 | Intron | XP_016864611.1 | ||||
XM_017009123.1 | Intron | XP_016864612.1 | ||||
XM_017009124.1 | Intron | XP_016864613.1 | ||||
XM_017009125.1 | Intron | XP_016864614.1 | ||||
XM_017009126.1 | Intron | XP_016864615.1 |