Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCTCGGCGCCTCTGCGCGCGGGAAG[A/G]TGGCGGAACAGGCTACCAAGTCCGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 171500 | ||||||||||||||||||||
Literature Links: |
ACP1 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap |
---|---|---|
Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available |
EAS - Not Available | African American - Not Available | YRI (Yoruba) - Not Available |
SAS - Not Available | Chinese - Not Available | CHB (Han Chinese) - Not Available |
AFR - Not Available | Japanese - Not Available | JPT (Japanese) - Not Available |
EUR - Not Available | ||
AMR - Not Available |
ACP1 - acid phosphatase 1, soluble | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001040649.2 | 97 | Missense Mutation | ATG,GTG | M,V 1 | NP_001035739.1 | |
NM_004300.3 | 97 | Intron | NP_004291.1 | |||
NM_007099.3 | 97 | Intron | NP_009030.1 |
SH3YL1 - SH3 and SYLF domain containing 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159597.2 | 97 | Intron | NP_001153069.1 | |||
NM_001282682.1 | 97 | Intron | NP_001269611.1 | |||
NM_001282687.1 | 97 | Intron | NP_001269616.1 | |||
NM_015677.3 | 97 | Intron | NP_056492.2 |