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GAATTCACTGTCTGCTTTTCCAAGT[C/T]ATACAGGCGCAGGGATATCTACTGA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616464 | ||||||||||||||||||||
Literature Links: |
ECD 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 |
ECD - ecdysoneless cell cycle regulator | ||||||
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There are no transcripts associated with this gene. |
FAM149B1 - family with sequence similarity 149 member B1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_173348.1 | 447 | Missense Mutation | CAT,TAT | H,Y 76 | NP_775483.1 | |
XM_005269744.2 | 447 | Missense Mutation | CAT,TAT | H,Y 76 | XP_005269801.1 | |
XM_005269745.2 | 447 | Missense Mutation | CAT,TAT | H,Y 76 | XP_005269802.1 | |
XM_005269747.3 | 447 | UTR 5 | XP_005269804.1 | |||
XM_011539737.2 | 447 | Silent Mutation | GTC,GTT | V,V 54 | XP_011538039.1 | |
XM_011539740.2 | 447 | Missense Mutation | CAT,TAT | H,Y 76 | XP_011538042.1 | |
XM_017016164.1 | 447 | Silent Mutation | GTC,GTT | V,V 54 | XP_016871653.1 | |
XM_017016165.1 | 447 | Intron | XP_016871654.1 | |||
XM_017016166.1 | 447 | Intron | XP_016871655.1 | |||
XM_017016167.1 | 447 | Missense Mutation | CAT,TAT | H,Y 76 | XP_016871656.1 |