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GGCGTCCTGGGCCAGTGCCCGCTCC[A/G]TGGTCAAGCTCATCGGCATCACGGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
FAM78A 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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FAM78A - family with sequence similarity 78 member A | ||||||
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There are no transcripts associated with this gene. |
PLPP7 - phospholipid phosphatase 7 (inactive) | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032728.3 | 650 | Missense Mutation | ATG,GTG | M,V 112 | NP_116117.3 | |
XM_005272230.3 | 650 | Missense Mutation | ATG,GTG | M,V 112 | XP_005272287.1 | |
XM_005272231.1 | 650 | Missense Mutation | ATG,GTG | M,V 112 | XP_005272288.1 |