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TGGATGAGCGTGGCCGCCCGTACCA[C/T]GCGCACCATCTCCTGCTCTGCCTCC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
IQCD 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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IQCD - IQ motif containing D | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_138451.2 | 859 | Missense Mutation | ATG,GTG | M,V 298 | NP_612460.1 | |
XM_005253832.4 | 859 | Missense Mutation | ATG,GTG | M,V 400 | XP_005253889.1 | |
XM_005253833.4 | 859 | Missense Mutation | ATG,GTG | M,V 400 | XP_005253890.1 | |
XM_005253834.4 | 859 | Missense Mutation | ATG,GTG | M,V 219 | XP_005253891.1 | |
XM_011537862.2 | 859 | Missense Mutation | ATG,GTG | M,V 400 | XP_011536164.1 | |
XM_011537863.2 | 859 | Missense Mutation | ATG,GTG | M,V 400 | XP_011536165.1 | |
XM_011537864.1 | 859 | Missense Mutation | ATG,GTG | M,V 322 | XP_011536166.1 | |
XM_011537865.2 | 859 | Missense Mutation | ATG,GTG | M,V 141 | XP_011536167.1 | |
XM_011537866.2 | 859 | Missense Mutation | ATG,GTG | M,V 60 | XP_011536168.1 | |
XM_017018771.1 | 859 | Missense Mutation | ATG,GTG | M,V 117 | XP_016874260.1 |
RITA1 - RBPJ interacting and tubulin associated 1 | ||||||
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There are no transcripts associated with this gene. |