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AATAGGAATCTCTGATGCTTACCTG[A/C]ACCCAACTTATCTTTCATAGCCCTC
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
|
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Phenotype: |
MIM: 603702 | ||||||||||||||||||||
Literature Links: |
NUP210L 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 |
NUP210L - nucleoporin 210 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001159484.1 | 5455 | Intron | NP_001152956.1 | |||
NM_207308.2 | 5455 | Missense Mutation | GCA,TCA | A,S 1795 | NP_997191.2 | |
XM_011510122.1 | 5455 | Missense Mutation | GCA,TCA | A,S 1751 | XP_011508424.1 | |
XM_011510123.1 | 5455 | Missense Mutation | GCA,TCA | A,S 1742 | XP_011508425.1 | |
XM_011510124.1 | 5455 | Intron | XP_011508426.1 | |||
XM_017002788.1 | 5455 | Missense Mutation | GCA,TCA | A,S 1795 | XP_016858277.1 | |
XM_017002789.1 | 5455 | Intron | XP_016858278.1 |
RPS27 - ribosomal protein S27 | ||||||
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There are no transcripts associated with this gene. |