Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGGTGCTCACGCAGCGTTGTGGGC[A/G]GCGGCCGGGCCGCAGAGAGCGCCGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
BREA2 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 |
BREA2 - breast cancer estrogen-induced apoptosis 2 | ||||||
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There are no transcripts associated with this gene. |
ZNF707 - zinc finger protein 707 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001100598.1 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | NP_001094068.1 | |
NM_001100599.1 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | NP_001094069.1 | |
NM_001288805.1 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | NP_001275734.1 | |
NM_001288806.1 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | NP_001275735.1 | |
NM_001288807.1 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | NP_001275736.1 | |
NM_001288808.1 | 717 | Missense Mutation | CAG,CGG | Q,R 123 | NP_001275737.1 | |
NM_001288809.1 | 717 | Missense Mutation | CAG,CGG | Q,R 123 | NP_001275738.1 | |
NM_173831.3 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | NP_776192.2 | |
XM_005250883.3 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | XP_005250940.1 | |
XM_006716542.3 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | XP_006716605.1 | |
XM_006716543.3 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | XP_006716606.1 | |
XM_011516977.2 | 717 | Missense Mutation | CAG,CGG | Q,R 159 | XP_011515279.1 | |
XM_011516979.2 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | XP_011515281.1 | |
XM_017013335.1 | 717 | Missense Mutation | CAG,CGG | Q,R 86 | XP_016868824.1 |