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Search Thermo Fisher Scientific
TAGCTGTGGCGGGTCAGCTTCTTCA[A/G]TATCTACTGTTTTTATCAACTCTGC
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 | |||
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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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TMEM168 - transmembrane protein 168 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001287497.1 | 2122 | Missense Mutation | ACT,ATT | T,I 577 | NP_001274426.1 | |
NM_022484.5 | 2122 | Missense Mutation | ACT,ATT | T,I 577 | NP_071929.3 | |
XM_017012523.1 | 2122 | Missense Mutation | ACT,ATT | T,I 577 | XP_016868012.1 | |
XM_017012524.1 | 2122 | Intron | XP_016868013.1 | |||
XM_017012525.1 | 2122 | Missense Mutation | ACT,ATT | T,I 193 | XP_016868014.1 |