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AGTTCCTGGACCCCAGCAAAAGCAG[C/T]GTGGGTATGTAGCCCTTACTCAAGG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609362 MIM: 605641 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
PLA2G15 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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PLA2G15 - phospholipase A2 group XV | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_012320.3 | 551 | Silent Mutation | AGC,AGT | S,S 133 | NP_036452.1 | |
XM_005255886.3 | 551 | Silent Mutation | AGC,AGT | S,S 133 | XP_005255943.1 | |
XM_011522979.2 | 551 | Silent Mutation | AGC,AGT | S,S 165 | XP_011521281.1 | |
XM_011522980.2 | 551 | Missense Mutation | GCG,GTG | A,V 25 | XP_011521282.2 |
SLC7A6 - solute carrier family 7 member 6 | ||||||
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There are no transcripts associated with this gene. |