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TCCCCACCACCATACATTTCTGCTA[C/G]CTTATTAAACCGAGGGCCCCATTCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604555 | ||||||||||||||||||||
Literature Links: |
CDH10 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 |
CDH10 - cadherin 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317222.1 | 2326 | Missense Mutation | CTA,GTA | L,V 181 | NP_001304151.1 | |
NM_001317224.1 | 2326 | Missense Mutation | CTA,GTA | L,V 773 | NP_001304153.1 | |
NM_006727.4 | 2326 | Missense Mutation | CTA,GTA | L,V 775 | NP_006718.2 | |
XM_011513923.2 | 2326 | Missense Mutation | CTA,GTA | L,V 775 | XP_011512225.1 | |
XM_017008915.1 | 2326 | Missense Mutation | CTA,GTA | L,V 773 | XP_016864404.1 |