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AGGAGTTACAGTGATGTCCCGGGGG[G/T]GCCAGCCTTGCTGGGGGATGCCCTT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
NUGGC 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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NUGGC - nuclear GTPase, germinal center associated | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001010906.1 | 1345 | Missense Mutation | ACC,CCC | T,P 791 | NP_001010906.1 | |
XM_011544523.2 | 1345 | Intron | XP_011542825.1 | |||
XM_011544524.2 | 1345 | Intron | XP_011542826.1 | |||
XM_011544525.1 | 1345 | Missense Mutation | ACC,CCC | T,P 404 | XP_011542827.1 | |
XM_011544526.2 | 1345 | Intron | XP_011542828.1 | |||
XM_017013403.1 | 1345 | Intron | XP_016868892.1 |