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Search Thermo Fisher Scientific
CAAATGGTCTTGTTCCCTTGCTCAC[A/C]TGATGATACGGCTGTGATGGAAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 603604 | ||||||||||||||||||||||||||||||||
Literature Links: |
PLA2G6 PubMed Links | ||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global - Not Available | Caucasian - Not Available | CEPH (CEU)
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EAS - Not Available | African American - Not Available | YRI (Yoruba)
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SAS - Not Available | Chinese - Not Available | JPT (Japanese)
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AFR - Not Available | Japanese - Not Available | CHB (Han Chinese)
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EUR - Not Available | |||||
AMR - Not Available |
PLA2G6 - phospholipase A2 group VI | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001004426.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | NP_001004426.1 | |
NM_001199562.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | NP_001186491.1 | |
NM_003560.2 | 772 | Missense Mutation | AGC,ATC | S,I 142 | NP_003551.2 | |
XM_005261764.2 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_005261821.1 | |
XM_005261765.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_005261822.1 | |
XM_005261766.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_005261823.1 | |
XM_006724332.3 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_006724395.1 | |
XM_011530422.1 | 772 | Missense Mutation | AGA,ATA | R,I 142 | XP_011528724.1 | |
XM_011530423.1 | 772 | UTR 5 | XP_011528725.1 | |||
XM_011530424.1 | 772 | UTR 5 | XP_011528726.1 | |||
XM_011530425.1 | 772 | UTR 5 | XP_011528727.1 | |||
XM_011530426.2 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_011528728.1 | |
XM_017028981.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_016884470.1 | |
XM_017028982.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_016884471.1 | |
XM_017028983.1 | 772 | UTR 5 | XP_016884472.1 | |||
XM_017028984.1 | 772 | UTR 5 | XP_016884473.1 | |||
XM_017028985.1 | 772 | UTR 5 | XP_016884474.1 | |||
XM_017028986.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_016884475.1 | |
XM_017028987.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_016884476.1 | |
XM_017028988.1 | 772 | Missense Mutation | AGC,ATC | S,I 142 | XP_016884477.1 |
Set Membership: |
HapMap |