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TGAGCTGGAAGTACTCCTTAGGCTG[A/G]AGGATGTCAAAGGGCTTCAGTTCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 300217 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RAI2 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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RAI2 - retinoic acid induced 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001172732.1 | 1527 | Silent Mutation | CTC,CTT | L,L 244 | NP_001166203.1 | |
NM_001172739.1 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | NP_001166210.1 | |
NM_001172743.1 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | NP_001166214.1 | |
NM_021785.4 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | NP_068557.3 | |
XM_006724459.2 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | XP_006724522.1 | |
XM_006724460.1 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | XP_006724523.1 | |
XM_011545439.2 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | XP_011543741.1 | |
XM_011545440.2 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | XP_011543742.1 | |
XM_011545441.2 | 1527 | Silent Mutation | CTC,CTT | L,L 294 | XP_011543743.1 |