Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GGTGATCGCCGTCTTCCAGCGCAAG[A/G]GGCTGCCCGACCAGGAGCTCTTCAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609406 | ||||||||||||||||||||
Literature Links: |
PRR5 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 |
PRR5 - proline rich 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001017528.2 | 588 | Missense Mutation | AGG,GGG | R,G 49 | NP_001017528.1 | |
NM_001017529.2 | 588 | UTR 5 | NP_001017529.1 | |||
NM_001017530.1 | 588 | UTR 5 | NP_001017530.1 | |||
NM_001198721.1 | 588 | Missense Mutation | AGG,GGG | R,G 81 | NP_001185650.1 | |
NM_015366.3 | 588 | Missense Mutation | AGG,GGG | R,G 49 | NP_056181.2 | |
NM_181333.3 | 588 | Missense Mutation | AGG,GGG | R,G 58 | NP_851850.1 |
PRR5-ARHGAP8 - PRR5-ARHGAP8 readthrough | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_181334.5 | 588 | Missense Mutation | AGG,GGG | R,G 58 | NP_851851.3 |