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CCGTGTGCTTGCAGCTGCTCCTGGA[A/C]CACCTGGAGTGCCTGGTGTCCAGGC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603144 | ||||||||||||||||||||
Literature Links: |
C19orf73 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 |
C19orf73 - chromosome 19 open reading frame 73 | ||||||
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There are no transcripts associated with this gene. |
PPFIA3 - PTPRF interacting protein alpha 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003660.3 | 703 | Missense Mutation | GAA,GAC | E,D 118 | NP_003651.1 | |
XM_017027407.1 | 703 | Missense Mutation | GAA,GAC | E,D 118 | XP_016882896.1 |