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GAGCTCTTGAGTGAGACCCAACAAG[C/T]TGCTTTTCACCAAATTGCAATGGAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604870 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
MARCO 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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MARCO - macrophage receptor with collagenous structure | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_006770.3 | 191 | Missense Mutation | GCT,GTT | A,V 19 | NP_006761.1 | |
XM_011512082.1 | 191 | Missense Mutation | GCT,GTT | A,V 19 | XP_011510384.1 | |
XM_011512083.2 | 191 | Missense Mutation | GCT,GTT | A,V 19 | XP_011510385.1 | |
XM_017005171.1 | 191 | Missense Mutation | GCT,GTT | A,V 19 | XP_016860660.1 |