Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 604912 | ||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
TAF2 PubMed Links | ||||||||||||||||||||||||||||||||||||||||||||
Allele Nomenclature: |
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Minor Allele Frequency: |
1000Genome | Applied Biosystems® | HapMap | ||||||
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Global
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Caucasian - Not Available | CEPH (CEU)
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EAS
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African American - Not Available | YRI (Yoruba)
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SAS
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Chinese - Not Available | CHB (Han Chinese) - Not Available | ||||||
AFR
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Japanese - Not Available | JPT (Japanese) - Not Available | ||||||
EUR
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AMR
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TAF2 - TATA-box binding protein associated factor 2 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_003184.3 | 3551 | Missense Mutation | ACA,GCA | T,A 1139 | NP_003175.1 | |
XM_006716621.3 | 3551 | Missense Mutation | ACA,GCA | T,A 1191 | XP_006716684.1 | |
XM_011517259.2 | 3551 | Missense Mutation | ACA,GCA | T,A 1154 | XP_011515561.1 | |
XM_017013779.1 | 3551 | Missense Mutation | ACA,GCA | T,A 1102 | XP_016869268.1 | |
XM_017013780.1 | 3551 | Missense Mutation | ACA,GCA | T,A 1022 | XP_016869269.1 | |
XM_017013781.1 | 3551 | Missense Mutation | ACA,GCA | T,A 1022 | XP_016869270.1 | |
XM_017013782.1 | 3551 | Missense Mutation | ACA,GCA | T,A 1022 | XP_016869271.1 | |
XM_017013783.1 | 3551 | Missense Mutation | ACA,GCA | T,A 980 | XP_016869272.1 | |
XM_017013784.1 | 3551 | Missense Mutation | ACA,GCA | T,A 970 | XP_016869273.1 | |
XM_017013785.1 | 3551 | Missense Mutation | ACA,GCA | T,A 970 | XP_016869274.1 | |
XM_017013786.1 | 3551 | Missense Mutation | ACA,GCA | T,A 970 | XP_016869275.1 | |
XM_017013787.1 | 3551 | Missense Mutation | ACA,GCA | T,A 933 | XP_016869276.1 | |
XM_017013788.1 | 3551 | Missense Mutation | ACA,GCA | T,A 774 | XP_016869277.1 | |
XM_017013789.1 | 3551 | Missense Mutation | ACA,GCA | T,A 722 | XP_016869278.1 | |
XM_017013790.1 | 3551 | Missense Mutation | ACA,GCA | T,A 722 | XP_016869279.1 | |
XM_017013791.1 | 3551 | Missense Mutation | ACA,GCA | T,A 692 | XP_016869280.1 |
Set Membership: |
HapMap |