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ATAGACGAAGCTTCTGGACTTCATT[C/G]TTTTACAAGCATTGATCGTTTCATC
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 |
---|---|---|
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 |
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 | 4732 | Missense Mutation | ACA,AGA | T,R 1473 | NP_001238949.1 | |
NM_001252024.1 | 4732 | Missense Mutation | ACA,AGA | T,R 1456 | NP_001238953.1 | |
NM_001252030.1 | 4732 | Intron | NP_001238959.1 | |||
NM_002420.5 | 4732 | Missense Mutation | ACA,AGA | T,R 1434 | NP_002411.3 |