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AGAAGGCTATCCCTGTCCTGCCACT[A/G]ATATAAAGGGATCAAAAGAATGTTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 143089 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
FOXN2 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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FOXN2 - forkhead box N2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002158.3 | Intron | NP_002149.2 | ||||
XM_005264282.2 | Intron | XP_005264339.1 | ||||
XM_005264283.2 | Intron | XP_005264340.1 | ||||
XM_006712001.3 | Intron | XP_006712064.1 | ||||
XM_006712002.3 | Intron | XP_006712065.1 | ||||
XM_011532808.2 | Intron | XP_011531110.1 | ||||
XM_017003956.1 | Intron | XP_016859445.1 | ||||
XM_017003957.1 | Intron | XP_016859446.1 | ||||
XM_017003958.1 | Intron | XP_016859447.1 | ||||
XM_017003959.1 | Intron | XP_016859448.1 |