Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGCAAATCTTGCTCTCCCACAGGAG[C/T]CTTCCAGGTAGGTACAAGGTATTAT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 147138 | ||||||||||||||||||||
Literature Links: |
MS4A2 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 |
MS4A2 - membrane spanning 4-domains A2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_000139.4 | 466 | Missense Mutation | CCT,TCT | P,S 17 | NP_000130.1 | |
NM_001256916.1 | 466 | Missense Mutation | CCT,TCT | P,S 17 | NP_001243845.1 | |
XM_005273846.4 | 466 | Missense Mutation | CCT,TCT | P,S 24 | XP_005273903.1 | |
XM_011544850.2 | 466 | Missense Mutation | CCT,TCT | P,S 17 | XP_011543152.1 | |
XM_017017362.1 | 466 | Missense Mutation | CCT,TCT | P,S 24 | XP_016872851.1 |