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ACCTACTGGCAGTTGAACATCAAGG[A/G]GTGAAACTGCTTGAAAACAGACATC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
MIER3 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 |
MIER3 - MIER family member 3 | ||||||
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There are no transcripts associated with this gene. |
SETD9 - SET domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001171990.2 | 688 | Silent Mutation | GGA,GGG | G,G 96 | NP_001165461.1 | |
NM_001323018.1 | 688 | Silent Mutation | GGA,GGG | G,G 70 | NP_001309947.1 | |
NM_001323019.1 | 688 | Silent Mutation | GGA,GGG | G,G 96 | NP_001309948.1 | |
NM_001323020.1 | 688 | Silent Mutation | GGA,GGG | G,G 70 | NP_001309949.1 | |
NM_001323022.1 | 688 | UTR 5 | NP_001309951.1 | |||
NM_153706.3 | 688 | Silent Mutation | GGA,GGG | G,G 96 | NP_714917.2 | |
XM_005248426.4 | 688 | Intron | XP_005248483.1 | |||
XM_011543139.2 | 688 | Silent Mutation | GGA,GGG | G,G 64 | XP_011541441.1 | |
XM_011543140.2 | 688 | Silent Mutation | GGA,GGG | G,G 20 | XP_011541442.1 |