Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ACGTCCTGCAAATGCAGTGCCTCTC[A/G]GATCTGGTGCAGCGACCCTTCTCCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600456 | ||||||||||||||||||||
Literature Links: |
NTRK2 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 |
NTRK2 - neurotrophic receptor tyrosine kinase 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001007097.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001007098.1 | |
NM_001018064.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001018074.1 | |
NM_001018065.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001018075.1 | |
NM_001018066.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001018076.1 | |
NM_001291937.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_001278866.1 | |
NM_006180.4 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | NP_006171.2 | |
XM_005252001.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_005252058.1 | |
XM_005252003.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_005252060.1 | |
XM_005252004.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_005252061.1 | |
XM_005252006.3 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_005252063.1 | |
XM_005252007.3 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_005252064.1 | |
XM_011518718.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_011517020.1 | |
XM_011518720.2 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_011517022.1 | |
XM_017014751.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870240.1 | |
XM_017014752.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870241.1 | |
XM_017014753.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870242.1 | |
XM_017014754.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870243.1 | |
XM_017014755.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870244.1 | |
XM_017014756.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870245.1 | |
XM_017014757.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870246.1 | |
XM_017014758.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870247.1 | |
XM_017014759.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870248.1 | |
XM_017014760.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870249.1 | |
XM_017014761.1 | 1037 | Missense Mutation | CAG,CGG | Q,R 42 | XP_016870250.1 |