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TCATGTGGCTGCCATTGTTGAAATG[A/G]CCTTCATTGGAGCCATACTGCTTAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603581 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCDH9 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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PCDH9 - protocadherin 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001318372.1 | 4301 | Silent Mutation | GGC,GGT | G,G 1161 | NP_001305301.1 | |
NM_001318373.1 | 4301 | Silent Mutation | GGC,GGT | G,G 1127 | NP_001305302.1 | |
NM_001318374.1 | 4301 | Intron | NP_001305303.1 | |||
NM_020403.4 | 4301 | Silent Mutation | GGC,GGT | G,G 1169 | NP_065136.1 | |
NM_203487.2 | 4301 | Silent Mutation | GGC,GGT | G,G 1203 | NP_982354.1 | |
XM_005266408.3 | 4301 | Intron | XP_005266465.1 | |||
XM_011535099.2 | 4301 | Intron | XP_011533401.1 | |||
XM_017020619.1 | 4301 | Silent Mutation | GGC,GGT | G,G 1203 | XP_016876108.1 | |
XM_017020620.1 | 4301 | Intron | XP_016876109.1 | |||
XM_017020621.1 | 4301 | Intron | XP_016876110.1 |