Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCTTCAAGAGCTGGAGGCTACAGT[G/T]CCCCTTCGGCAACAATGACAAGGTA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603749 | ||||||||||||||||||||
Literature Links: |
TRPM2 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 |
TRPM2 - transient receptor potential cation channel subfamily M member 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320350.1 | 648 | Missense Mutation | TGC,TTC | C,F 48 | NP_001307279.1 | |
NM_001320351.1 | 648 | Missense Mutation | TGC,TTC | C,F 48 | NP_001307280.1 | |
NM_001320352.1 | 648 | Intron | NP_001307281.1 | |||
NM_003307.3 | 648 | Missense Mutation | TGC,TTC | C,F 48 | NP_003298.1 | |
XM_005261171.3 | 648 | Missense Mutation | TGC,TTC | C,F 48 | XP_005261228.1 | |
XM_011529736.2 | 648 | Missense Mutation | TGC,TTC | C,F 48 | XP_011528038.1 | |
XM_017028456.1 | 648 | Missense Mutation | TGC,TTC | C,F 48 | XP_016883945.1 | |
XM_017028457.1 | 648 | Missense Mutation | TGC,TTC | C,F 48 | XP_016883946.1 |