Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
AGAACTTGGCTCAGCGTGCTTTCTC[A/G]GGCTAGGAGGGTAAAGGGCATGCCG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 605405 | ||||||||||||||||||||
Literature Links: |
USP6NL 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 |
USP6NL - USP6 N-terminal like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080491.3 | 5183 | Missense Mutation | CCG,CTG | P,L 603 | NP_001073960.1 | |
NM_014688.3 | 5183 | Missense Mutation | CCG,CTG | P,L 586 | NP_055503.1 | |
XM_006717542.3 | 5183 | Missense Mutation | CCG,CTG | P,L 614 | XP_006717605.1 | |
XM_011519762.2 | 5183 | Missense Mutation | CCG,CTG | P,L 614 | XP_011518064.1 | |
XM_011519763.2 | 5183 | Missense Mutation | CCG,CTG | P,L 430 | XP_011518065.1 | |
XM_017016971.1 | 5183 | Missense Mutation | CCG,CTG | P,L 604 | XP_016872460.1 | |
XM_017016972.1 | 5183 | Missense Mutation | CCG,CTG | P,L 430 | XP_016872461.1 | |
XM_017016973.1 | 5183 | Missense Mutation | CCG,CTG | P,L 609 | XP_016872462.1 |