Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCGAACCAAAAACAAATCCTGGCA[A/C]CTTGCCATTCCCAGAAAAGCCAGTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
PP12613 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 |
PP12613 - uncharacterized LOC100192379 | ||||||
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There are no transcripts associated with this gene. |
TMEM155 - transmembrane protein 155 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317837.1 | 699 | Missense Mutation | AGG,AGT | R,S 54 | NP_001304766.1 | |
NM_001317838.1 | 699 | Missense Mutation | AGG,AGT | R,S 54 | NP_001304767.1 | |
NM_001317839.1 | 699 | Missense Mutation | AGG,AGT | R,S 54 | NP_001304768.1 | |
NM_001317841.1 | 699 | Missense Mutation | AGG,AGT | R,S 28 | NP_001304770.1 | |
NM_001317842.1 | 699 | Missense Mutation | AGG,AGT | R,S 28 | NP_001304771.1 | |
NM_152399.3 | 699 | Missense Mutation | AGG,AGT | R,S 54 | NP_689612.3 | |
XM_005262737.2 | 699 | Missense Mutation | AGG,AGT | R,S 54 | XP_005262794.1 | |
XM_017007725.1 | 699 | Missense Mutation | AGG,AGT | R,S 54 | XP_016863214.1 | |
XM_017007726.1 | 699 | Missense Mutation | AGG,AGT | R,S 28 | XP_016863215.1 |