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TCCAAAGGCTTCTAAGCATGCGGGA[A/G]AAGAAGGTAAGCACTAAAACGTCCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 611690 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PRRG4 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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PRRG4 - proline rich and Gla domain 4 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_024081.5 | 208 | Missense Mutation | AAA,GAA | K,E 33 | NP_076986.1 | |
XM_006718313.3 | 208 | Missense Mutation | AAA,GAA | K,E 171 | XP_006718376.3 | |
XM_006718314.3 | 208 | Missense Mutation | AAA,GAA | K,E 33 | XP_006718377.1 | |
XM_017018275.1 | 208 | Missense Mutation | AAA,GAA | K,E 171 | XP_016873764.1 |