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CGCTGTGCTTCCTGGCATTTTGGAG[A/G]CACACATTTTGGGAACACCCCCATG
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602246 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
TOB2P1 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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TOB2P1 - transducer of ERBB2, 2 pseudogene 1 | ||||||
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There are no transcripts associated with this gene. |
ZSCAN9 - zinc finger and SCAN domain containing 9 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001199479.1 | 560 | Intron | NP_001186408.1 | |||
NM_001199480.1 | 560 | Intron | NP_001186409.1 | |||
NM_006299.4 | 560 | Intron | NP_006290.1 | |||
XM_011514875.2 | 560 | Missense Mutation | GAC,GGC | D,G 97 | XP_011513177.1 | |
XM_011514876.2 | 560 | Missense Mutation | GAC,GGC | D,G 97 | XP_011513178.1 | |
XM_011514878.2 | 560 | Missense Mutation | GAC,GGC | D,G 97 | XP_011513180.1 | |
XM_017011267.1 | 560 | Intron | XP_016866756.1 |