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CTGTTGGTGGGTGAGCGGGCCATGC[A/G]AGGCTGCTGTGGTGGCTGCTGGCCA
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 607396 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TOB2 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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TOB2 - transducer of ERBB2, 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_016272.3 | 1876 | Missense Mutation | CGC,TGC | R,C 218 | NP_057356.1 | |
XM_005261315.2 | 1876 | Missense Mutation | CGC,TGC | R,C 218 | XP_005261372.1 | |
XM_006724105.3 | 1876 | Missense Mutation | CGC,TGC | R,C 218 | XP_006724168.1 | |
XM_017028539.1 | 1876 | Missense Mutation | CGC,TGC | R,C 218 | XP_016884028.1 |