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GAAGCTTGCAGCGTCACTGCCTTCT[G/T]CCAGTGGAGCGGGACTGTGTTTTTT
Species: |
Human | |||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600374 | |||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
BBS4 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)
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SAS
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Chinese - Not Available | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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BBS4 - Bardet-Biedl syndrome 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252678.1 | Intron | NP_001239607.1 | ||||
NM_001320665.1 | Intron | NP_001307594.1 | ||||
NM_033028.4 | Intron | NP_149017.2 | ||||
XM_011521848.1 | Intron | XP_011520150.1 | ||||
XM_011521849.1 | Intron | XP_011520151.1 | ||||
XM_011521851.1 | Intron | XP_011520153.1 | ||||
XM_017022450.1 | Intron | XP_016877939.1 | ||||
XM_017022451.1 | Intron | XP_016877940.1 | ||||
XM_017022452.1 | Intron | XP_016877941.1 | ||||
XM_017022453.1 | Intron | XP_016877942.1 | ||||
XM_017022454.1 | Intron | XP_016877943.1 |
HIGD2B - HIG1 hypoxia inducible domain family member 2B | ||||||
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There are no transcripts associated with this gene. |