Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
TGGCGGCCCCGCAGCCTCTCACACC[A/G]GGCTCCCGTGAGGTCAAGGAGGGCT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606088 MIM: 605916 | ||||||||||||||||||||
Literature Links: |
JMJD7-PLA2G4B 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 |
JMJD7-PLA2G4B - JMJD7-PLA2G4B readthrough | ||||||
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There are no transcripts associated with this gene. |
PLA2G4B - phospholipase A2 group IVB | ||||||
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There are no transcripts associated with this gene. |
SPTBN5 - spectrin beta, non-erythrocytic 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016642.3 | 10989 | Silent Mutation | NP_057726.4 | |||
XM_017022299.1 | 10989 | Missense Mutation | XP_016877788.1 | |||
XM_017022300.1 | 10989 | Missense Mutation | XP_016877789.1 | |||
XM_017022301.1 | 10989 | Missense Mutation | XP_016877790.1 | |||
XM_017022302.1 | 10989 | Missense Mutation | XP_016877791.1 | |||
XM_017022303.1 | 10989 | Intron | XP_016877792.1 | |||
XM_017022304.1 | 10989 | Intron | XP_016877793.1 | |||
XM_017022305.1 | 10989 | Intron | XP_016877794.1 |