Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCAGGTCACCCCGTGAAGCTAATC[C/G]TCGAGATTCCAGTTGAATATTTCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603651 | ||||||||||||||||||||
Literature Links: |
TRPC4 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 |
TRPC4 - transient receptor potential cation channel subfamily C member 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001135955.1 | 3464 | Missense Mutation | CGA,GGA | R,G 806 | NP_001129427.1 | |
NM_001135956.1 | 3464 | Missense Mutation | CGA,GGA | R,G 741 | NP_001129428.1 | |
NM_001135957.1 | 3464 | Missense Mutation | CGA,GGA | R,G 749 | NP_001129429.1 | |
NM_001135958.1 | 3464 | Missense Mutation | CGA,GGA | R,G 717 | NP_001129430.1 | |
NM_003306.1 | 3464 | Missense Mutation | CGA,GGA | R,G 895 | NP_003297.1 | |
NM_016179.2 | 3464 | Missense Mutation | CGA,GGA | R,G 890 | NP_057263.1 | |
XM_011535206.1 | 3464 | Missense Mutation | CGA,GGA | R,G 475 | XP_011533508.1 | |
XM_017020723.1 | 3464 | Missense Mutation | CGA,GGA | R,G 475 | XP_016876212.1 | |
XM_017020724.1 | 3464 | Missense Mutation | CGA,GGA | R,G 470 | XP_016876213.1 |