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TCACTTCTTTGAAAAATATATGCCT[C/T]TTAGAAAGCTGAACATTAGAAAATA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606200 MIM: 601599 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BHLHE41 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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BHLHE41 - basic helix-loop-helix family member e41 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030762.2 | 2329 | UTR 3 | NP_110389.1 |
SSPN - sarcospan | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135823.1 | 2329 | Intron | NP_001129295.1 | |||
NM_005086.4 | 2329 | Intron | NP_005077.2 | |||
XM_011520853.2 | 2329 | Intron | XP_011519155.1 | |||
XM_011520854.2 | 2329 | Intron | XP_011519156.1 | |||
XM_011520855.2 | 2329 | Intron | XP_011519157.1 |