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GGCAGCAAGTCCTAGAACTGGAAAA[A/G]GAATTTCATTTTAACAGGTATCTGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142980 MIM: 142981 MIM: 611576 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
HOXD3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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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HOXD3 - homeobox D3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006898.4 | 762 | Intron | NP_008829.3 | |||
XM_005246509.3 | 762 | Intron | XP_005246566.1 | |||
XM_005246510.4 | 762 | Intron | XP_005246567.1 | |||
XM_005246511.3 | 762 | Intron | XP_005246568.1 | |||
XM_005246513.4 | 762 | Intron | XP_005246570.1 | |||
XM_006712477.2 | 762 | Intron | XP_006712540.1 | |||
XM_011511065.2 | 762 | Intron | XP_011509367.1 | |||
XM_011511066.2 | 762 | Intron | XP_011509368.1 |
HOXD4 - homeobox D4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_014621.2 | 762 | Silent Mutation | AAA,AAG | K,K 171 | NP_055436.2 | |
XM_005246514.4 | 762 | Intron | XP_005246571.1 |
MIR10B - microRNA 10b | ||||||
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There are no transcripts associated with this gene. |