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TGGGAAAAGTTGTATCTGTAATAGT[C/T]CTTGTAGATGCTGCACCCCTGGGTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 605630 | ||||||||||||||||||||
Literature Links: |
PLA2G2D 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 |
PLA2G2D - phospholipase A2 group IID | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001271814.1 | 318 | Intron | NP_001258743.1 | |||
NM_012400.3 | 318 | Missense Mutation | AAC,GAC | N,D 84 | NP_036532.1 |