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TCAACAGCATCTGCATTGCCGGGAC[C/T]GGATATGAGCATGAAACCTAGTGCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 606471 MIM: 608963 MIM: 604878 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
NOP10 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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NOP10 - NOP10 ribonucleoprotein | ||||||
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There are no transcripts associated with this gene. |
NUTM1 - NUT midline carcinoma family member 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001284292.1 | 501 | Missense Mutation | CCG,CTG | P,L 40 | NP_001271221.1 | |
NM_001284293.1 | 501 | Missense Mutation | CCG,CTG | P,L 30 | NP_001271222.1 | |
NM_175741.2 | 501 | Missense Mutation | CCG,CTG | P,L 12 | NP_786883.1 |
SLC12A6 - solute carrier family 12 member 6 | ||||||
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There are no transcripts associated with this gene. |