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AGGCAGCGTGCCGTCCCTGGCTGCA[G/T]GGCTGCTCTTCGGCAGTCTAGCCGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TMEM14B 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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TMEM14B - transmembrane protein 14B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001127711.2 | 291 | Intron | NP_001121183.1 | |||
NM_001286484.1 | 291 | Intron | NP_001273413.1 | |||
NM_001286488.1 | 291 | Missense Mutation | GGG,TGG | G,W 42 | NP_001273417.1 | |
NM_001286489.1 | 291 | Intron | NP_001273418.1 | |||
NM_030969.4 | 291 | Intron | NP_112231.3 |