Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CACTCACCTCCTAGAGACCAGGCTG[A/C]CATCATGCTCTGGAAGCTTGTGGAG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 601601 | ||||||||||||||||||||
Literature Links: |
TFAP2B 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 |
TFAP2B - transcription factor AP-2 beta | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003221.3 | 467 | Missense Mutation | GAC,GCC | D,A 10 | NP_003212.2 | |
XM_011514837.2 | 467 | Missense Mutation | GAC,GCC | D,A 10 | XP_011513139.1 | |
XM_017011233.1 | 467 | Missense Mutation | ACA,CCA | T,P 41 | XP_016866722.1 | |
XM_017011234.1 | 467 | Missense Mutation | ACA,CCA | T,P 29 | XP_016866723.1 | |
XM_017011235.1 | 467 | Missense Mutation | GAC,GCC | D,A 10 | XP_016866724.1 |