Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAAGGGCAGGTGGGTGCGGCCGTG[C/G]GGGTGCTGGGGGTGCGGCGCCCCAA
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 |
---|---|---|
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 |
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 | 1638 | Silent Mutation | CCC,CCG | P,P 449 | NP_110389.1 |
SSPN - sarcospan | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135823.1 | 1638 | Intron | NP_001129295.1 | |||
NM_005086.4 | 1638 | Intron | NP_005077.2 | |||
XM_011520853.2 | 1638 | Intron | XP_011519155.1 | |||
XM_011520854.2 | 1638 | Intron | XP_011519156.1 | |||
XM_011520855.2 | 1638 | Intron | XP_011519157.1 |