Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GCCAACTTGTCTAGTTTCTTAAAGG[G/T]CCCTCCCAGTCGAACAGGGGAAGCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605514 | ||||||||||||||||||||
Literature Links: |
PCDH15 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 |
PCDH15 - protocadherin related 15 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001142763.1 | 5121 | Intron | NP_001136235.1 | |||
NM_001142764.1 | 5121 | Intron | NP_001136236.1 | |||
NM_001142765.1 | 5121 | Intron | NP_001136237.1 | |||
NM_001142766.1 | 5121 | Intron | NP_001136238.1 | |||
NM_001142767.1 | 5121 | Intron | NP_001136239.1 | |||
NM_001142768.1 | 5121 | Intron | NP_001136240.1 | |||
NM_001142769.1 | 5121 | Intron | NP_001136241.1 | |||
NM_001142770.1 | 5121 | Intron | NP_001136242.1 | |||
NM_001142771.1 | 5121 | Missense Mutation | ACC,CCC | T,P 1576 | NP_001136243.1 | |
NM_001142772.1 | 5121 | Missense Mutation | ACC,CCC | T,P 1571 | NP_001136244.1 | |
NM_001142773.1 | 5121 | Intron | NP_001136245.1 | |||
NM_033056.3 | 5121 | Intron | NP_149045.3 | |||
XM_017016571.1 | 5121 | Missense Mutation | ACC,CCC | T,P 1612 | XP_016872060.1 | |
XM_017016572.1 | 5121 | Missense Mutation | ACC,CCC | T,P 1569 | XP_016872061.1 | |
XM_017016573.1 | 5121 | Intron | XP_016872062.1 |