Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
ATAGGCACTGTTCTCTGACAATCCT[C/T]CTTGGCACTGTTTATCGACTGGTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
1 submissions
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Phenotype: |
MIM: 607860 | ||||||||||||||||||||
Literature Links: |
YY1AP1 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 |
YY1AP1 - YY1 associated protein 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198899.1 | 2675 | Missense Mutation | GAA,GGA | E,G 679 | NP_001185828.1 | |
NM_001198900.1 | 2675 | Missense Mutation | GAA,GGA | E,G 679 | NP_001185829.1 | |
NM_001198901.1 | 2675 | Missense Mutation | GAA,GGA | E,G 690 | NP_001185830.1 | |
NM_001198902.1 | 2675 | Missense Mutation | GAA,GGA | E,G 690 | NP_001185831.1 | |
NM_001198903.1 | 2675 | Missense Mutation | GAA,GGA | E,G 828 | NP_001185832.1 | |
NM_001198904.1 | 2675 | Missense Mutation | GAA,GGA | E,G 808 | NP_001185833.1 | |
NM_001198905.1 | 2675 | Missense Mutation | GAA,GGA | E,G 670 | NP_001185834.1 | |
NM_001198906.1 | 2675 | UTR 3 | NP_001185835.1 | |||
NM_018253.3 | 2675 | Missense Mutation | GAA,GGA | E,G 679 | NP_060723.2 | |
NM_139118.2 | 2675 | Missense Mutation | GAA,GGA | E,G 736 | NP_620829.1 | |
NM_139119.2 | 2675 | Missense Mutation | GAA,GGA | E,G 690 | NP_620830.1 | |
NM_139121.2 | 2675 | Missense Mutation | GAA,GGA | E,G 624 | NP_620832.1 |