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AGTGATCCTCCCACCTCAGCTTCTC[A/G]AATAGTTGTGTCTACAGGCGCGTGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606586 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC105374753 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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LOC105374753 - uncharacterized LOC105374753 | ||||||
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There are no transcripts associated with this gene. |
RAI14 - retinoic acid induced 14 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145520.1 | Intron | NP_001138992.1 | ||||
NM_001145521.1 | Intron | NP_001138993.1 | ||||
NM_001145522.1 | Intron | NP_001138994.1 | ||||
NM_001145523.1 | Intron | NP_001138995.1 | ||||
NM_001145525.1 | Intron | NP_001138997.1 | ||||
NM_015577.2 | Intron | NP_056392.2 | ||||
XM_006714469.2 | Intron | XP_006714532.1 | ||||
XM_011514016.2 | Intron | XP_011512318.2 | ||||
XM_011514017.2 | Intron | XP_011512319.1 | ||||
XM_011514018.1 | Intron | XP_011512320.1 | ||||
XM_011514019.1 | Intron | XP_011512321.1 | ||||
XM_011514020.1 | Intron | XP_011512322.1 | ||||
XM_011514021.1 | Intron | XP_011512323.1 | ||||
XM_011514022.1 | Intron | XP_011512324.1 | ||||
XM_011514023.1 | Intron | XP_011512325.1 | ||||
XM_011514024.1 | Intron | XP_011512326.1 | ||||
XM_011514025.2 | Intron | XP_011512327.2 | ||||
XM_017009334.1 | Intron | XP_016864823.1 | ||||
XM_017009335.1 | Intron | XP_016864824.1 | ||||
XM_017009336.1 | Intron | XP_016864825.1 |