Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AATCAAGAGACTTACTGATTTCTTT[C/T]TGTGAAACTTGTATGATGCTGGCAG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 109090 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
METTL5 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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METTL5 - methyltransferase like 5 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001293186.1 | 774 | Missense Mutation | AAA,AGA | K,R 194 | NP_001280115.1 | |
NM_001293187.1 | 774 | Missense Mutation | AAA,AGA | K,R 194 | NP_001280116.1 | |
NM_014168.3 | 774 | Missense Mutation | AAA,AGA | K,R 194 | NP_054887.2 | |
XM_011511023.1 | 774 | Missense Mutation | AAA,GAA | K,E 177 | XP_011509325.1 |
SSB - Sjogren syndrome antigen B | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001294145.1 | 774 | Intron | NP_001281074.1 | |||
NM_003142.4 | 774 | Intron | NP_003133.1 |