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GCTCATGGTAAATGCCACTGACCCT[A/G]ATGAGGGAGCCAATGGGGAAGTAAC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606288 MIM: 606289 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PCDHGA1 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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PCDHGA1 - protocadherin gamma subfamily A, 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_018912.2 | 808 | Missense Mutation | AAT,GAT | N,D 270 | NP_061735.1 | |
NM_031993.1 | 808 | Missense Mutation | AAT,GAT | N,D 270 | NP_114382.1 |
PCDHGA2 - protocadherin gamma subfamily A, 2 | ||||||
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There are no transcripts associated with this gene. |