Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AAACAGAGAGAGTCTGGTTTTATAT[C/T]CCTGCGAATTTTGTTCTCCTCAATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 600562 | ||||||||||||||||||||
Literature Links: |
CDH12 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 |
CDH12 - cadherin 12 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001317227.1 | 2788 | Missense Mutation | AAT,GAT | N,D 692 | NP_001304156.1 | |
NM_001317228.1 | 2788 | Missense Mutation | AAT,GAT | N,D 652 | NP_001304157.1 | |
NM_004061.4 | 2788 | Missense Mutation | AAT,GAT | N,D 692 | NP_004052.2 | |
XM_011513927.2 | 2788 | Missense Mutation | AAT,GAT | N,D 692 | XP_011512229.1 | |
XM_017008920.1 | 2788 | Missense Mutation | AAT,GAT | N,D 692 | XP_016864409.1 | |
XM_017008921.1 | 2788 | Missense Mutation | AAT,GAT | N,D 692 | XP_016864410.1 |