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TGAGAAAGAGTCATACTTGGAGAGT[C/T]GCAGCAGTGGGGCCCAACAGTCACT
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 616856 | ||||||||||||||||||||
Literature Links: |
BRPF3 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 |
BRPF3 - bromodomain and PHD finger containing 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_015695.2 | 828 | Missense Mutation | CGC,TGC | R,C 200 | NP_056510.2 | |
XM_005249010.2 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_005249067.1 | |
XM_005249011.3 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_005249068.1 | |
XM_011514489.1 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_011512791.1 | |
XM_011514490.1 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_011512792.1 | |
XM_011514491.1 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_011512793.1 | |
XM_011514492.1 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_011512794.1 | |
XM_017010742.1 | 828 | Missense Mutation | CGC,TGC | R,C 200 | XP_016866231.1 | |
XM_017010743.1 | 828 | Intron | XP_016866232.1 |
LOC102723648 - uncharacterized LOC102723648 | ||||||
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There are no transcripts associated with this gene. |