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CATTCTGGTGGGCTTTACCGAAGGC[A/G]GGTGGGGACGGGCTCTCGTAGCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
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Phenotype: |
MIM: 142967 MIM: 142966 | ||||||||||||||||||||
Literature Links: |
HOXB-AS1 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 |
HOXB-AS1 - HOXB cluster antisense RNA 1 | ||||||
---|---|---|---|---|---|---|
There are no transcripts associated with this gene. |
HOXB2 - homeobox B2 | ||||||
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There are no transcripts associated with this gene. |
HOXB3 - homeobox B3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_002146.4 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | NP_002137.4 | |
XM_005257277.3 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | XP_005257334.1 | |
XM_005257280.3 | 11274 | Silent Mutation | CCC,CCT | P,P 219 | XP_005257337.1 | |
XM_005257282.3 | 11274 | Silent Mutation | CCC,CCT | P,P 160 | XP_005257339.1 | |
XM_006721854.2 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | XP_006721917.1 | |
XM_011524707.2 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_011523009.1 | |
XM_011524708.2 | 11274 | Silent Mutation | CCC,CCT | P,P 349 | XP_011523010.1 | |
XM_011524710.1 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | XP_011523012.1 | |
XM_011524719.1 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | XP_011523021.1 | |
XM_011524720.2 | 11274 | Silent Mutation | CCC,CCT | P,P 292 | XP_011523022.1 | |
XM_011524721.2 | 11274 | Silent Mutation | CCC,CCT | P,P 291 | XP_011523023.1 | |
XM_011524726.2 | 11274 | Silent Mutation | CCC,CCT | P,P 219 | XP_011523028.1 | |
XM_017024557.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880046.1 | |
XM_017024558.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880047.1 | |
XM_017024559.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880048.1 | |
XM_017024560.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880049.1 | |
XM_017024561.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880050.1 | |
XM_017024562.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880051.1 | |
XM_017024563.1 | 11274 | Silent Mutation | CCC,CCT | P,P 439 | XP_016880052.1 |