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GTCCCAGGGCAGATCCAAGTTTCAT[A/G]GAACTTGGATATTATACACTTTTGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604148 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
RPS7P1 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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RPS7P1 - ribosomal protein S7 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |
SLC13A2 - solute carrier family 13 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001145975.1 | Intron | NP_001139447.1 | ||||
NM_003984.3 | Intron | NP_003975.1 | ||||
XM_006722165.2 | Intron | XP_006722228.1 | ||||
XM_011525450.2 | Intron | XP_011523752.1 | ||||
XM_011525451.1 | Intron | XP_011523753.1 | ||||
XM_011525452.1 | Intron | XP_011523754.1 | ||||
XM_011525453.2 | Intron | XP_011523755.1 | ||||
XM_011525454.2 | Intron | XP_011523756.1 |