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Search Thermo Fisher Scientific
GAAGTCAGAGTAAGCCTGTTTCCAC[C/T]GCAGCACAGCAGTGAGCACAGCTAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606548 | ||||||||||||||||||||
Literature Links: |
MS4A6A 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 |
MS4A6A - membrane spanning 4-domains A6A | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001247999.1 | 884 | Missense Mutation | CAG,CGG | Q,R 235 | NP_001234928.1 | |
NM_022349.3 | 884 | Missense Mutation | CAG,CGG | Q,R 207 | NP_071744.2 | |
NM_152851.2 | 884 | Silent Mutation | GCA,GCG | A,A 172 | NP_690590.1 | |
NM_152852.2 | 884 | Missense Mutation | CAG,CGG | Q,R 207 | NP_690591.1 | |
XM_005274177.2 | 884 | Missense Mutation | CAG,CGG | Q,R 235 | XP_005274234.1 | |
XM_006718658.2 | 884 | Missense Mutation | CAG,CGG | Q,R 235 | XP_006718721.1 | |
XM_006718660.2 | 884 | Missense Mutation | CAG,CGG | Q,R 190 | XP_006718723.1 | |
XM_006718661.2 | 884 | Missense Mutation | CAG,CGG | Q,R 190 | XP_006718724.1 | |
XM_011545209.1 | 884 | Intron | XP_011543511.1 | |||
XM_017018123.1 | 884 | Missense Mutation | CAG,CGG | Q,R 162 | XP_016873612.1 | |
XM_017018124.1 | 884 | Missense Mutation | CAG,CGG | Q,R 162 | XP_016873613.1 | |
XM_017018125.1 | 884 | Intron | XP_016873614.1 |