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AAGCGGAGGAGGGGGCGGCGGCCGA[A/C]GGGGGAGGGGGGCTGTCGTTTGAGT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 104155 | ||||||||||||||||||||
Literature Links: |
ZFHX3 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 |
ZFHX3 - zinc finger homeobox 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001164766.1 | 8187 | Silent Mutation | CCG,CCT | P,P 2686 | NP_001158238.1 | |
NM_006885.3 | 8187 | Silent Mutation | CCG,CCT | P,P 3600 | NP_008816.3 | |
XM_005255957.3 | 8187 | Silent Mutation | CCG,CCT | P,P 3599 | XP_005256014.1 | |
XM_017023251.1 | 8187 | Silent Mutation | CCG,CCT | P,P 2717 | XP_016878740.1 |