Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CGAACGACGGAGTCTTTTCCTTTCT[C/T]GTCGATGCAGTTTCTCAGCCTCCTG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616197 | ||||||||||||||||||||
Literature Links: |
NOL10 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 |
NOL10 - nucleolar protein 10 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001261392.1 | 1645 | Missense Mutation | CAA,CGA | Q,R 639 | NP_001248321.1 | |
NM_001261394.1 | 1645 | Missense Mutation | CAA,CGA | Q,R 615 | NP_001248323.1 | |
NM_024894.3 | 1645 | Missense Mutation | CAA,CGA | Q,R 665 | NP_079170.2 | |
XM_011510398.2 | 1645 | Missense Mutation | CAA,CGA | Q,R 515 | XP_011508700.1 | |
XM_011510399.2 | 1645 | Missense Mutation | CAA,CGA | Q,R 515 | XP_011508701.1 | |
XM_011510400.2 | 1645 | Intron | XP_011508702.1 | |||
XM_011510402.2 | 1645 | Intron | XP_011508704.1 | |||
XM_017004990.1 | 1645 | Missense Mutation | CAA,CGA | Q,R 340 | XP_016860479.1 | |
XM_017004991.1 | 1645 | Missense Mutation | CAA,CGA | Q,R 340 | XP_016860480.1 |