Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGGCCCACCTTGCGCATGCACTGCC[C/T]CTCCACGTTGCAGCGACACACGATC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603118 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDH16 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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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
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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CDH16 - cadherin 16 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001204744.1 | 2387 | Missense Mutation | AGG,GGG | R,G 746 | NP_001191673.1 | |
NM_001204745.1 | 2387 | Missense Mutation | AGG,GGG | R,G 729 | NP_001191674.1 | |
NM_001204746.1 | 2387 | Missense Mutation | AGG,GGG | R,G 671 | NP_001191675.1 | |
NM_004062.3 | 2387 | Missense Mutation | AGG,GGG | R,G 768 | NP_004053.1 | |
XM_005255770.2 | 2387 | Missense Mutation | AGG,GGG | R,G 590 | XP_005255827.1 | |
XM_011522807.1 | 2387 | Missense Mutation | AGG,GGG | R,G 705 | XP_011521109.1 |