Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TCGGAAGTGGCATGGGCGTACTGTC[C/T]GTAGAGATCAGCATTCTGGATGTAT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 608500 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRICKLE1 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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PRICKLE1 - prickle planar cell polarity protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001144881.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | NP_001138353.1 | |
NM_001144882.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | NP_001138354.1 | |
NM_001144883.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | NP_001138355.1 | |
NM_153026.2 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | NP_694571.2 | |
XM_011537946.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | XP_011536248.1 | |
XM_011537947.2 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | XP_011536249.1 | |
XM_017018838.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | XP_016874327.1 | |
XM_017018839.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | XP_016874328.1 | |
XM_017018840.1 | 2299 | Missense Mutation | AGA,GGA | R,G 732 | XP_016874329.1 |