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TGGTGTGCCGTGGTGACCCCCTGAG[A/C]TCCCCTATAAAATGTTGGCCTCTAT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601740 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
LOC145845 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 | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese)
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EUR
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AMR
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LOC145845 - uncharacterized LOC145845 | ||||||
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There are no transcripts associated with this gene. |
MEIS2 - Meis homeobox 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001220482.1 | Intron | NP_001207411.1 | ||||
NM_002399.3 | Intron | NP_002390.1 | ||||
NM_170674.4 | Intron | NP_733774.1 | ||||
NM_170675.4 | Intron | NP_733775.1 | ||||
NM_170676.4 | Intron | NP_733776.1 | ||||
NM_170677.4 | Intron | NP_733777.1 | ||||
NM_172315.2 | Intron | NP_758526.1 | ||||
NM_172316.2 | Intron | NP_758527.1 | ||||
XM_006720523.1 | Intron | XP_006720586.1 | ||||
XM_006720524.1 | Intron | XP_006720587.1 | ||||
XM_006720525.1 | Intron | XP_006720588.1 | ||||
XM_006720526.2 | Intron | XP_006720589.1 | ||||
XM_006720527.2 | Intron | XP_006720590.1 | ||||
XM_006720529.2 | Intron | XP_006720592.1 | ||||
XM_011521591.2 | Intron | XP_011519893.1 | ||||
XM_017022205.1 | Intron | XP_016877694.1 |
Set Membership: |
HapMap |