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CTGGAATGTAGTTCCTTGTGTGGCA[A/T]CTTATTTCTAATGTAGAAAAAACAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603356 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CD164 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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CD164 - CD164 molecule | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142401.1 | 712 | UTR 3 | NP_001135873.1 | |||
NM_001142402.1 | 712 | UTR 3 | NP_001135874.1 | |||
NM_001142403.1 | 712 | Missense Mutation | AGA,AGT | R,S 177 | NP_001135875.1 | |
NM_001142404.1 | 712 | Missense Mutation | AGA,AGT | R,S 145 | NP_001135876.1 | |
NM_006016.4 | 712 | UTR 3 | NP_006007.2 |