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GGGTCACGGCGCAGGACCACGGCAT[C/G]CCCCGACGAAGTGCCCTGGCTACAC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
13 submissions
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Phenotype: |
MIM: 604265 | ||||||||||||||||||||
Literature Links: |
CELSR2 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 |
CELSR2 - cadherin EGF LAG seven-pass G-type receptor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001408.2 | 859 | Missense Mutation | ATC,ATG | I,M 266 | NP_001399.1 | |
XM_005270580.4 | 859 | Missense Mutation | ATC,ATG | I,M 266 | XP_005270637.1 |