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CCTTGGATGGACAGCTAGGGGATCC[C/T]GTGTTTTGCTGCTGCAAAGGACATT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607642 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAI1 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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RAI1 - retinoic acid induced 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030665.3 | Intron | NP_109590.3 | ||||
XM_017024025.1 | Intron | XP_016879514.1 | ||||
XM_017024026.1 | Intron | XP_016879515.1 | ||||
XM_017024027.1 | Intron | XP_016879516.1 | ||||
XM_017024028.1 | Intron | XP_016879517.1 |
SMCR5 - Smith-Magenis syndrome chromosome region, candidate 5 (non-protein coding) | ||||||
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There are no transcripts associated with this gene. |