Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CAGCATGATTTCACAGCTCTGGTCG[C/T]TTTTTTCCCACATGTCGGTTCCTTC
Species: |
Human | ||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
24 submissions
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Phenotype: |
MIM: 604704 MIM: 608848 | ||||||||||||||||||||||||||||||||||||||
Literature Links: |
BCAR3 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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
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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BCAR3 - breast cancer anti-estrogen resistance 3 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001261408.1 | 2089 | Missense Mutation | AAC,AGC | N,S 733 | NP_001248337.1 | |
NM_001261409.1 | 2089 | Missense Mutation | AAC,AGC | N,S 733 | NP_001248338.1 | |
NM_001261410.1 | 2089 | Missense Mutation | AAC,AGC | N,S 642 | NP_001248339.1 | |
NM_001308251.1 | 2089 | Missense Mutation | AAC,AGC | N,S 409 | NP_001295180.1 | |
NM_003567.3 | 2089 | Missense Mutation | AAC,AGC | N,S 733 | NP_003558.1 | |
XM_011542251.2 | 2089 | Missense Mutation | AAC,AGC | N,S 513 | XP_011540553.1 | |
XM_017002480.1 | 2089 | Missense Mutation | AAC,AGC | N,S 733 | XP_016857969.1 |
FNBP1L - formin binding protein 1 like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001024948.2 | 2089 | Intron | NP_001020119.1 | |||
NM_001164473.2 | 2089 | Intron | NP_001157945.1 | |||
NM_017737.4 | 2089 | Intron | NP_060207.2 | |||
XM_011541625.2 | 2089 | Intron | XP_011539927.1 | |||
XM_017001533.1 | 2089 | Intron | XP_016857022.1 |