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ACGGAGAGCTGGACTTCACGGGGGC[C/T]GGCCGCAAGCACAGCAATGTGAGGC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606936 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TRPM4 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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TRPM4 - transient receptor potential cation channel subfamily M member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001195227.1 | 357 | Silent Mutation | GCC,GCT | A,A 83 | NP_001182156.1 | |
NM_001321281.1 | 357 | Silent Mutation | GCC,GCT | A,A 83 | NP_001308210.1 | |
NM_001321282.1 | 357 | UTR 5 | NP_001308211.1 | |||
NM_001321283.1 | 357 | Intron | NP_001308212.1 | |||
NM_001321285.1 | 357 | Intron | NP_001308214.1 | |||
NM_017636.3 | 357 | Silent Mutation | GCC,GCT | A,A 83 | NP_060106.2 | |
XM_005259017.1 | 357 | Intron | XP_005259074.1 |