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Search Thermo Fisher Scientific
GTGGGTCAGTACTTGGACAGCCATC[C/T]GTTTCTGGCCTTCACCTTGCTGGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611304 | ||||||||||||||||||||
Literature Links: |
TMEM159 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 |
TMEM159 - transmembrane protein 159 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001301769.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | NP_001288698.1 | |
NM_001301771.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | NP_001288700.1 | |
NM_001301773.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | NP_001288702.1 | |
NM_001301774.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | NP_001288703.1 | |
NM_001301775.1 | 821 | Missense Mutation | CCG,CTG | P,L 73 | NP_001288704.1 | |
NM_020422.5 | 821 | Missense Mutation | CCG,CTG | P,L 49 | NP_065155.3 | |
XM_005255439.4 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_005255496.1 | |
XM_006721066.2 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_006721129.1 | |
XM_006721067.3 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_006721130.1 | |
XM_006721069.3 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_006721132.1 | |
XM_017023471.1 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_016878960.1 | |
XM_017023472.1 | 821 | Missense Mutation | CCG,CTG | P,L 73 | XP_016878961.1 | |
XM_017023473.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | XP_016878962.1 | |
XM_017023474.1 | 821 | Missense Mutation | CCG,CTG | P,L 49 | XP_016878963.1 |