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TTGAGTTGATCAAAAAAGAACTCAT[A/G]GCCATTAATTTCTGGGAATTGCCCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 142966 MIM: 142965 MIM: 610173 | ||||||||||||||||||||
Literature Links: |
HOXB3 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
HOXB3 - homeobox B3 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002146.4 | 68 | Intron | NP_002137.4 | |||
XM_005257277.3 | 68 | Intron | XP_005257334.1 | |||
XM_005257280.3 | 68 | Intron | XP_005257337.1 | |||
XM_005257282.3 | 68 | Intron | XP_005257339.1 | |||
XM_006721854.2 | 68 | Intron | XP_006721917.1 | |||
XM_011524707.2 | 68 | Intron | XP_011523009.1 | |||
XM_011524708.2 | 68 | Intron | XP_011523010.1 | |||
XM_011524710.1 | 68 | Intron | XP_011523012.1 | |||
XM_011524719.1 | 68 | Intron | XP_011523021.1 | |||
XM_011524720.2 | 68 | Intron | XP_011523022.1 | |||
XM_011524721.2 | 68 | Intron | XP_011523023.1 | |||
XM_011524726.2 | 68 | Intron | XP_011523028.1 | |||
XM_017024557.1 | 68 | Intron | XP_016880046.1 | |||
XM_017024558.1 | 68 | Intron | XP_016880047.1 | |||
XM_017024559.1 | 68 | Intron | XP_016880048.1 | |||
XM_017024560.1 | 68 | Intron | XP_016880049.1 | |||
XM_017024561.1 | 68 | Intron | XP_016880050.1 | |||
XM_017024562.1 | 68 | Intron | XP_016880051.1 | |||
XM_017024563.1 | 68 | Intron | XP_016880052.1 |
HOXB4 - homeobox B4 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024015.4 | 68 | Silent Mutation | GCC,GCT | A,A 2 | NP_076920.1 |
MIR10A - microRNA 10a | ||||||
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There are no transcripts associated with this gene. |