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CTTTAGGCAACATGGCGAACTAGAC[A/G]TCCAAGTACGAAAAGGACAGAGTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 613483 MIM: 603711 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BHLHE22 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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BHLHE22 - basic helix-loop-helix family member e22 | ||||||
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There are no transcripts associated with this gene. |
CYP7B1 - cytochrome P450 family 7 subfamily B member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001324112.1 | 5192 | Intron | NP_001311041.1 | |||
NM_004820.4 | 5192 | UTR 3 | NP_004811.1 | |||
XM_017014002.1 | 5192 | UTR 3 | XP_016869491.1 |