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TGCCAGCCACACTGGTCACGAGGTT[C/G]CCAGGGAACGTGAACAGAACCCTTT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616251 | ||||||||||||||||||||
Literature Links: |
TCAF1 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 |
TCAF1 - TRPM8 channel associated factor 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001206938.1 | 855 | Silent Mutation | GGC,GGG | G,G 172 | NP_001193867.1 | |
NM_001206941.1 | 855 | Intron | NP_001193870.1 | |||
NM_014719.2 | 855 | Silent Mutation | GGC,GGG | G,G 172 | NP_055534.1 | |
XM_005250074.3 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_005250131.1 | |
XM_005250075.2 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_005250132.1 | |
XM_005250076.3 | 855 | Intron | XP_005250133.1 | |||
XM_005250077.2 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_005250134.1 | |
XM_006716191.2 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_006716254.1 | |
XM_006716192.3 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_006716255.1 | |
XM_017012833.1 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_016868322.1 | |
XM_017012834.1 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_016868323.1 | |
XM_017012835.1 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_016868324.1 | |
XM_017012836.1 | 855 | Silent Mutation | GGC,GGG | G,G 172 | XP_016868325.1 |