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TTTTGCTGGAATAAGGGATAAAGAC[A/G]GGTAAAGCTTTGTTTTTTGTTGTTG
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 | |||
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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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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 | Intron | NP_001234928.1 | ||||
NM_022349.3 | Intron | NP_071744.2 | ||||
NM_152851.2 | Intron | NP_690590.1 | ||||
NM_152852.2 | Intron | NP_690591.1 | ||||
XM_005274177.2 | Intron | XP_005274234.1 | ||||
XM_006718658.2 | Intron | XP_006718721.1 | ||||
XM_006718660.2 | Intron | XP_006718723.1 | ||||
XM_006718661.2 | Intron | XP_006718724.1 | ||||
XM_011545209.1 | Intron | XP_011543511.1 | ||||
XM_017018123.1 | Intron | XP_016873612.1 | ||||
XM_017018124.1 | Intron | XP_016873613.1 | ||||
XM_017018125.1 | Intron | XP_016873614.1 |