Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TTCTGTAACATGATGTGTTGATTGG[C/T]TGTGTTAATGTTGGTCCCTGGAATA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
|
||||||||||||||||||||
Phenotype: |
MIM: 601690 MIM: 611200 | ||||||||||||||||||||
Literature Links: |
PLA2G7 PubMed Links | ||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||
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 |
PLA2G7 - phospholipase A2 group VII | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001168357.1 | 1451 | Missense Mutation | ACC,GCC | T,A 425 | NP_001161829.1 | |
NM_005084.3 | 1451 | Missense Mutation | ACC,GCC | T,A 425 | NP_005075.3 | |
XM_005249408.4 | 1451 | Missense Mutation | ACC,GCC | T,A 425 | XP_005249465.1 |
TDRD6 - tudor domain containing 6 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010870.2 | 1451 | Intron | NP_001010870.1 | |||
NM_001168359.1 | 1451 | Intron | NP_001161831.1 |