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AACTTCGTGGACCCAGCTGCCTCCT[C/T]GTCGGCTGAAGACAGCCTGTCAGAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600840 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
LINC01184 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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LINC01184 - long intergenic non-protein coding RNA 1184 | ||||||
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There are no transcripts associated with this gene. |
SLC12A2 - solute carrier family 12 member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001046.2 | 613 | Missense Mutation | TCG,TTG | S,L 150 | NP_001037.1 | |
NM_001256461.1 | 613 | Missense Mutation | TCG,TTG | S,L 150 | NP_001243390.1 | |
XM_011543588.2 | 613 | Missense Mutation | TCG,TTG | S,L 150 | XP_011541890.1 | |
XM_017009771.1 | 613 | Intron | XP_016865260.1 |