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GGATCTTCACCTTCCACTCCATGCG[C/T]GGCTCCGACGGGGTGGGAGAGCTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609729 | ||||||||||||||||||||
Literature Links: |
PDZRN3 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 |
PDZRN3 - PDZ domain containing ring finger 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001303139.1 | 2191 | Silent Mutation | CCA,CCG | P,P 615 | NP_001290068.1 | |
NM_001303140.1 | 2191 | Silent Mutation | CCA,CCG | P,P 574 | NP_001290069.1 | |
NM_001303141.1 | 2191 | Silent Mutation | CCA,CCG | P,P 639 | NP_001290070.1 | |
NM_001303142.1 | 2191 | Silent Mutation | CCA,CCG | P,P 634 | NP_001290071.1 | |
NM_015009.2 | 2191 | Silent Mutation | CCA,CCG | P,P 917 | NP_055824.1 | |
XM_017005942.1 | 2191 | Silent Mutation | CCA,CCG | P,P 888 | XP_016861431.1 |