Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTTTGTAAAGTCACCTAGCTGTGGC[A/G]GGTCAGCTTCTTCAATATCTACTGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
TMEM168 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 |
TMEM168 - transmembrane protein 168 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287497.1 | 2137 | Missense Mutation | CCG,CTG | P,L 582 | NP_001274426.1 | |
NM_022484.5 | 2137 | Missense Mutation | CCG,CTG | P,L 582 | NP_071929.3 | |
XM_017012523.1 | 2137 | Missense Mutation | CCG,CTG | P,L 582 | XP_016868012.1 | |
XM_017012524.1 | 2137 | Intron | XP_016868013.1 | |||
XM_017012525.1 | 2137 | Missense Mutation | CCG,CTG | P,L 198 | XP_016868014.1 |