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CGGGGGAGAAAGCGACGCGGCCGCT[C/T]GTAAGTGCTCCGGATGGAAACTGGT
Species: |
Human | ||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 609388 | ||||||||||||||||||||||||||||||||
Literature Links: |
LOC101927814 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 |
LOC101927814 - uncharacterized LOC101927814 | ||||||
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There are no transcripts associated with this gene. |
METTL9 - methyltransferase like 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001077180.2 | 8 | UTR 5 | NP_001070648.1 | |||
NM_001288659.1 | 8 | Intron | NP_001275588.1 | |||
NM_001288660.1 | 8 | Intron | NP_001275589.1 | |||
NM_016025.4 | 8 | UTR 5 | NP_057109.3 | |||
XM_017023269.1 | 8 | Intron | XP_016878758.1 |