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ACCCCAGTCACTGAGGTAGTCAAAA[C/T]TCTGGTCTGAGTCTGATGTGGTGGA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603008 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
CDH8 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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CDH8 - cadherin 8 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001796.4 | 2151 | Missense Mutation | AAT,AGT | N,S 772 | NP_001787.2 | |
XM_005255760.3 | 2151 | Intron | XP_005255817.1 | |||
XM_017022829.1 | 2151 | Missense Mutation | AAT,AGT | N,S 594 | XP_016878318.1 |