Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAATCAGTAGTGCAATTGCAACTAT[C/G]ATGATGCAAAATATCACACCAAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 300631 | ||||||||||||||||||||
Literature Links: |
TMEM27 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
TMEM27 - transmembrane protein 27 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_020665.5 | 718 | Missense Mutation | ATC,ATG | I,M 154 | NP_065716.1 | |
XM_017029680.1 | 718 | Missense Mutation | ATC,ATG | I,M 102 | XP_016885169.1 | |
XM_017029681.1 | 718 | Intron | XP_016885170.1 |