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CGGTATGAAGGTCACATCATGAGCC[A/G]CATAGAGATACAGCTTTCTGCAAGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
15 submissions
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Phenotype: |
MIM: 611471 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACP6 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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ACP6 - acid phosphatase 6, lysophosphatidic | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001323625.1 | 1459 | Missense Mutation | GCG,GTG | A,V 332 | NP_001310554.1 | |
NM_016361.4 | 1459 | Missense Mutation | GCG,GTG | A,V 332 | NP_057445.4 | |
XM_011509601.2 | 1459 | Missense Mutation | GCG,GTG | A,V 332 | XP_011507903.1 | |
XM_017001422.1 | 1459 | Missense Mutation | GCG,GTG | A,V 332 | XP_016856911.1 |