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CAAAGGCTCCAAGCTAAACCCATAA[A/G]AGACTGTCCTGTGAGAGCTTGGATG
Species: |
Human | ||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613667 | ||||||||||||||||||||||||||
Literature Links: |
SOBP PubMed Links | ||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR - Not Available | Japanese - Not Available | JPT (Japanese)
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EUR - Not Available | |||||
AMR - Not Available |
SOBP - sine oculis binding protein homolog | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018013.3 | Intron | NP_060483.3 | ||||
XM_005267041.4 | Intron | XP_005267098.1 | ||||
XM_005267042.4 | Intron | XP_005267099.1 | ||||
XM_011535920.2 | Intron | XP_011534222.1 | ||||
XM_011535921.2 | Intron | XP_011534223.1 | ||||
XM_011535923.2 | Intron | XP_011534225.1 | ||||
XM_017010991.1 | Intron | XP_016866480.1 | ||||
XM_017010992.1 | Intron | XP_016866481.1 | ||||
XM_017010993.1 | Intron | XP_016866482.1 | ||||
XM_017010994.1 | Intron | XP_016866483.1 |
Set Membership: |
HapMap |