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GTTTCTATGACTTTATTTTCTAACA[A/T]CTTCTTTAAATCTTTAGGCATAGCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
5 submissions
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Phenotype: |
MIM: 615255 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
C1orf112 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
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Global
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Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
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AMR
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C1orf112 - chromosome 1 open reading frame 112 | ||||||
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There are no transcripts associated with this gene. |
METTL18 - methyltransferase like 18 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001320199.1 | 593 | Missense Mutation | ATG,TTG | M,L 112 | NP_001307128.1 | |
NM_001320201.1 | 593 | Missense Mutation | ATG,TTG | M,L 112 | NP_001307130.1 | |
NM_033418.3 | 593 | Missense Mutation | ATG,TTG | M,L 112 | NP_219486.1 | |
XM_006711627.3 | 593 | Missense Mutation | ATG,TTG | M,L 112 | XP_006711690.1 |