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CTGGGCCTGATGACCGGACCTGTGG[A/G]GTAGATTCCGACGCGACTGGGTCAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
27 submissions
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Phenotype: |
MIM: 606066 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LHX9 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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LHX9 - LIM homeobox 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001014434.1 | Intron | NP_001014434.1 | ||||
NM_020204.2 | Intron | NP_064589.2 | ||||
XM_005245350.3 | Intron | XP_005245407.2 | ||||
XM_011509781.2 | Intron | XP_011508083.2 | ||||
XM_017001849.1 | Intron | XP_016857338.1 |