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TGCTGCCACAGAGGCTGATGGACAA[C/G]CAGGCGGAGAGAGAAAGTGAGGCTG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607256 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
APOL6 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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APOL6 - apolipoprotein L6 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_030641.3 | 303 | Missense Mutation | AAC,AAG | N,K 3 | NP_085144.1 | |
XM_011530392.2 | 303 | Missense Mutation | AAC,AAG | N,K 3 | XP_011528694.1 |