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TCTAACTTTCCCTGAATGGATTTCA[C/T]ATTCCTAGGATGTCCATGTAAACTT
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
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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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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 | 5109 | Missense Mutation | ATG,GTG | M,V 1599 | NP_001238949.1 | |
NM_001252024.1 | 5109 | Missense Mutation | ATG,GTG | M,V 1582 | NP_001238953.1 | |
NM_001252030.1 | 5109 | Intron | NP_001238959.1 | |||
NM_002420.5 | 5109 | Missense Mutation | ATG,GTG | M,V 1560 | NP_002411.3 |