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ACAGCAAACAGCACCACCGCTGCCA[C/T]CAGCAGACCTACCAGGAGCACAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605086 MIM: 609714 | ||||||||||||||||||||
Literature Links: |
LOC105375056 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 |
LOC105375056 - uncharacterized LOC105375056 | ||||||
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There are no transcripts associated with this gene. |
TREM2 - triggering receptor expressed on myeloid cells 2 | ||||||
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There are no transcripts associated with this gene. |
TREML1 - triggering receptor expressed on myeloid cells like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271807.1 | 584 | Missense Mutation | ATG,GTG | M,V 175 | NP_001258736.1 | |
NM_001271808.1 | 584 | Missense Mutation | ATG,GTG | M,V 64 | NP_001258737.1 | |
NM_178174.3 | 584 | Missense Mutation | ATG,GTG | M,V 175 | NP_835468.1 | |
XM_017010822.1 | 584 | Missense Mutation | ATG,GTG | M,V 234 | XP_016866311.1 | |
XM_017010823.1 | 584 | Missense Mutation | ATG,GTG | M,V 175 | XP_016866312.1 | |
XM_017010824.1 | 584 | Missense Mutation | ATG,GTG | M,V 175 | XP_016866313.1 | |
XM_017010825.1 | 584 | Missense Mutation | ATG,GTG | M,V 234 | XP_016866314.1 |