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TGTCCAGAGAGTGGAGAAGAGGCTG[G/T]GATTTTGCTGGAGGATCTGGAGAGA
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 |
---|---|---|
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 |
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 | 1011 | Missense Mutation | GGG,GTG | G,V 124 | NP_001186408.1 | |
NM_001199480.1 | 1011 | Missense Mutation | GGG,GTG | G,V 124 | NP_001186409.1 | |
NM_006299.4 | 1011 | Missense Mutation | GGG,GTG | G,V 124 | NP_006290.1 | |
XM_011514875.2 | 1011 | Missense Mutation | GGG,GTG | G,V 256 | XP_011513177.1 | |
XM_011514876.2 | 1011 | Missense Mutation | GGG,GTG | G,V 256 | XP_011513178.1 | |
XM_011514878.2 | 1011 | Missense Mutation | GGG,GTG | G,V 256 | XP_011513180.1 | |
XM_017011267.1 | 1011 | Missense Mutation | GGG,GTG | G,V 124 | XP_016866756.1 |