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GGTTGAGCACAGCCCGGACAGCCTC[A/G]GCGAACACTTCCTTGACACCATCCT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 615187 MIM: 179505 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PGAP2 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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PGAP2 - post-GPI attachment to proteins 2 | ||||||
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There are no transcripts associated with this gene. |
RHOG - ras homolog family member G | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001665.3 | 848 | Silent Mutation | GCC,GCT | A,A 170 | NP_001656.2 | |
XM_005252916.2 | 848 | Silent Mutation | GCC,GCT | A,A 170 | XP_005252973.1 | |
XM_017017719.1 | 848 | Silent Mutation | GCC,GCT | A,A 170 | XP_016873208.1 |