Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATGGTCTGTGCCCAGGTATTCATAG[A/C]CAAACTGAGCAGCAGGACACCCATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606411 | ||||||||||||||||||||
Literature Links: |
OCSTAMP 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 |
OCSTAMP - osteoclast stimulatory transmembrane protein | ||||||
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There are no transcripts associated with this gene. |
SLC13A3 - solute carrier family 13 member 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001011554.2 | 1551 | Missense Mutation | GCT,TCT | A,S 515 | NP_001011554.1 | |
NM_001193339.1 | 1551 | Missense Mutation | GCT,TCT | A,S 512 | NP_001180268.1 | |
NM_001193340.1 | 1551 | Missense Mutation | GCT,TCT | A,S 480 | NP_001180269.1 | |
NM_001193342.1 | 1551 | Missense Mutation | GCT,TCT | A,S 464 | NP_001180271.1 | |
NM_022829.5 | 1551 | Missense Mutation | GCT,TCT | A,S 562 | NP_073740.2 |