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CTTCTTTCAGGCCATCCAGATCCTG[A/T]ATGCAGCAATGATTCTGGCTTTGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606498 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MS4A3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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MS4A3 - membrane spanning 4-domains A3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001031666.1 | 47 | Intron | NP_001026836.1 | |||
NM_001031809.1 | 47 | Intron | NP_001026979.1 | |||
NM_006138.4 | 47 | Missense Mutation | AAT,TAT | N,Y 58 | NP_006129.4 | |
XM_011545363.2 | 47 | UTR 5 | XP_011543665.1 |