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GCCATTCCGTCGTCAATTGCTGGTC[C/T]GTGATTGAACTGTACTCTACATCCT
Species: |
Human | |||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603576 | |||||||||||||||||||||||
Literature Links: |
TRPM1 PubMed Links | |||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS - Not Available | African American - Not Available | YRI (Yoruba)
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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 |
TRPM1 - transient receptor potential cation channel subfamily M member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001252020.1 | 4817 | Silent Mutation | NP_001238949.1 | |||
NM_001252024.1 | 4817 | Silent Mutation | NP_001238953.1 | |||
NM_001252030.1 | 4817 | Intron | NP_001238959.1 | |||
NM_002420.5 | 4817 | Silent Mutation | NP_002411.3 |
Set Membership: |
HapMap |