Search Thermo Fisher Scientific
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TGAAGATCTCCCAGAGGATCACCCC[A/G]AAGCTCCATACATCACTCTCTGTAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 191316 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NTRK3 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
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
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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NTRK3 - neurotrophic receptor tyrosine kinase 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007156.2 | 2193 | Intron | NP_001007157.1 | |||
NM_001012338.2 | 2193 | Silent Mutation | TTC,TTT | F,F 756 | NP_001012338.1 | |
NM_001243101.1 | 2193 | Silent Mutation | TTC,TTT | F,F 734 | NP_001230030.1 | |
NM_001320134.1 | 2193 | Intron | NP_001307063.1 | |||
NM_001320135.1 | 2193 | Intron | NP_001307064.1 | |||
NM_002530.3 | 2193 | Silent Mutation | TTC,TTT | F,F 742 | NP_002521.2 | |
XM_006720543.3 | 2193 | Silent Mutation | TTC,TTT | F,F 742 | XP_006720606.1 | |
XM_006720544.3 | 2193 | Silent Mutation | TTC,TTT | F,F 734 | XP_006720607.1 | |
XM_006720545.3 | 2193 | Intron | XP_006720608.1 | |||
XM_006720548.3 | 2193 | Intron | XP_006720611.1 | |||
XM_006720549.3 | 2193 | Intron | XP_006720612.1 | |||
XM_006720550.3 | 2193 | Intron | XP_006720613.1 | |||
XM_011521637.2 | 2193 | Intron | XP_011519939.1 | |||
XM_011521638.2 | 2193 | Intron | XP_011519940.1 | |||
XM_017022240.1 | 2193 | Silent Mutation | TTC,TTT | F,F 742 | XP_016877729.1 | |
XM_017022241.1 | 2193 | Silent Mutation | TTC,TTT | F,F 680 | XP_016877730.1 | |
XM_017022242.1 | 2193 | Intron | XP_016877731.1 | |||
XM_017022243.1 | 2193 | Silent Mutation | TTC,TTT | F,F 644 | XP_016877732.1 | |
XM_017022244.1 | 2193 | Silent Mutation | TTC,TTT | F,F 644 | XP_016877733.1 | |
XM_017022245.1 | 2193 | Silent Mutation | TTC,TTT | F,F 644 | XP_016877734.1 | |
XM_017022246.1 | 2193 | Silent Mutation | TTC,TTT | F,F 644 | XP_016877735.1 | |
XM_017022247.1 | 2193 | Intron | XP_016877736.1 | |||
XM_017022248.1 | 2193 | Intron | XP_016877737.1 | |||
XM_017022249.1 | 2193 | Intron | XP_016877738.1 | |||
XM_017022250.1 | 2193 | Intron | XP_016877739.1 | |||
XM_017022251.1 | 2193 | Silent Mutation | TTC,TTT | F,F 373 | XP_016877740.1 | |
XM_017022252.1 | 2193 | Silent Mutation | TTC,TTT | F,F 365 | XP_016877741.1 | |
XM_017022253.1 | 2193 | Silent Mutation | TTC,TTT | F,F 756 | XP_016877742.1 | |
XM_017022254.1 | 2193 | Silent Mutation | TTC,TTT | F,F 767 | XP_016877743.1 |