Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GACAATCCTTCTTGGCACTGTTTAT[C/T]GACTGGTGGAGGCCCTGGGCTATGT
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
4 submissions
|
||||||||||||||||||||||||||||||||||||||
Phenotype: |
MIM: 607860 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
YY1AP1 PubMed Links | ||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
|||||||||||||||||||||||||||||||||||||||
Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | |||
---|---|---|---|---|---|
Global
|
Caucasian - Not Available | CEPH (CEU) - Not Available | |||
EAS
|
African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
Chinese - Not Available | CHB (Han Chinese) - Not Available | |||
AFR
|
Japanese - Not Available | JPT (Japanese) - Not Available | |||
EUR
|
|||||
AMR
|
YY1AP1 - YY1 associated protein 1 | ||||||
---|---|---|---|---|---|---|
Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001198899.1 | 2659 | Missense Mutation | AAT,GAT | N,D 674 | NP_001185828.1 | |
NM_001198900.1 | 2659 | Missense Mutation | AAT,GAT | N,D 674 | NP_001185829.1 | |
NM_001198901.1 | 2659 | Missense Mutation | AAT,GAT | N,D 685 | NP_001185830.1 | |
NM_001198902.1 | 2659 | Missense Mutation | AAT,GAT | N,D 685 | NP_001185831.1 | |
NM_001198903.1 | 2659 | Missense Mutation | AAT,GAT | N,D 823 | NP_001185832.1 | |
NM_001198904.1 | 2659 | Missense Mutation | AAT,GAT | N,D 803 | NP_001185833.1 | |
NM_001198905.1 | 2659 | Missense Mutation | AAT,GAT | N,D 665 | NP_001185834.1 | |
NM_001198906.1 | 2659 | UTR 3 | NP_001185835.1 | |||
NM_018253.3 | 2659 | Missense Mutation | AAT,GAT | N,D 674 | NP_060723.2 | |
NM_139118.2 | 2659 | Missense Mutation | AAT,GAT | N,D 731 | NP_620829.1 | |
NM_139119.2 | 2659 | Missense Mutation | AAT,GAT | N,D 685 | NP_620830.1 | |
NM_139121.2 | 2659 | Missense Mutation | AAT,GAT | N,D 619 | NP_620832.1 |