Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGTCTCAGGGGGAGGCTCGGATTTC[C/T]GGTGGGCTGCCACTGACAGGTCTAG
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 |
---|---|---|
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 |
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 | 1697 | Missense Mutation | NP_001166203.1 | |||
NM_001172739.1 | 1697 | Missense Mutation | NP_001166210.1 | |||
NM_001172743.1 | 1697 | Missense Mutation | NP_001166214.1 | |||
NM_021785.4 | 1697 | Missense Mutation | NP_068557.3 | |||
XM_006724459.2 | 1697 | Missense Mutation | XP_006724522.1 | |||
XM_006724460.1 | 1697 | Missense Mutation | XP_006724523.1 | |||
XM_011545439.2 | 1697 | Missense Mutation | XP_011543741.1 | |||
XM_011545440.2 | 1697 | Missense Mutation | XP_011543742.1 | |||
XM_011545441.2 | 1697 | Missense Mutation | XP_011543743.1 |