Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGCAGATAGCCGTTGGGGACCTTGC[A/G]CTGGTGCCGCTTTGAGGGGTCCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 171640 MIM: 612248 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
ACP5 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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ACP5 - acid phosphatase 5, tartrate resistant | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001111034.2 | 1217 | Missense Mutation | NP_001104504.1 | |||
NM_001111035.2 | 1217 | Missense Mutation | NP_001104505.1 | |||
NM_001111036.2 | 1217 | Missense Mutation | NP_001104506.1 | |||
NM_001322023.1 | 1217 | Missense Mutation | NP_001308952.1 | |||
NM_001611.4 | 1217 | Missense Mutation | NP_001602.1 | |||
XM_005259938.1 | 1217 | Missense Mutation | XP_005259995.1 | |||
XM_011528069.2 | 1217 | Missense Mutation | XP_011526371.1 |
ZNF627 - zinc finger protein 627 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001290083.1 | 1217 | Intron | NP_001277012.1 | |||
NM_001290084.1 | 1217 | Intron | NP_001277013.1 | |||
NM_001290085.1 | 1217 | Intron | NP_001277014.1 | |||
NM_145295.3 | 1217 | Intron | NP_660338.1 | |||
XM_011527780.2 | 1217 | Intron | XP_011526082.1 |