Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAGGGGCAGACATGCTGAATTCCA[C/T]GGGCGAACTGGAGTTTTCGAACGAA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NSUN7 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 |
NSUN7 - NOP2/Sun RNA methyltransferase family member 7 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
XM_017008611.1 | 532 | Missense Mutation | ACG,ATG | T,M 5 | XP_016864100.1 | |
XM_017008612.1 | 532 | Missense Mutation | ACG,ATG | T,M 5 | XP_016864101.1 | |
XM_017008613.1 | 532 | Missense Mutation | ACG,ATG | T,M 5 | XP_016864102.1 | |
XM_017008614.1 | 532 | Missense Mutation | ACG,ATG | T,M 5 | XP_016864103.1 | |
XM_017008615.1 | 532 | Missense Mutation | ACG,ATG | T,M 5 | XP_016864104.1 |