Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
Species: |
Human | ||||||||||||||||||||||||||||||||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 602968 | ||||||||||||||||||||||||||||||||||||||||||||||||||
Literature Links: |
BCAS1 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 | JPT (Japanese)
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AFR
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Japanese - Not Available | CHB (Han Chinese)
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EUR
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AMR
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BCAS1 - breast carcinoma amplified sequence 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001316361.2 | 1823 | Missense Mutation | CCC,TCC | P,S 505 | NP_001303290.1 | |
NM_001323347.1 | 1823 | Missense Mutation | CCC,TCC | P,S 505 | NP_001310276.1 | |
NM_003657.3 | 1823 | Missense Mutation | CCC,TCC | P,S 583 | NP_003648.2 | |
XM_005260587.2 | 1823 | Missense Mutation | CCC,TCC | P,S 628 | XP_005260644.1 | |
XM_005260589.2 | 1823 | Missense Mutation | CCC,TCC | P,S 614 | XP_005260646.1 | |
XM_005260590.2 | 1823 | Missense Mutation | CCC,TCC | P,S 606 | XP_005260647.1 | |
XM_005260591.2 | 1823 | Missense Mutation | CCC,TCC | P,S 592 | XP_005260648.1 | |
XM_005260593.2 | 1823 | Missense Mutation | CCC,TCC | P,S 569 | XP_005260650.1 | |
XM_005260594.2 | 1823 | Missense Mutation | CCC,TCC | P,S 550 | XP_005260651.1 | |
XM_005260595.2 | 1823 | Missense Mutation | CCC,TCC | P,S 536 | XP_005260652.1 | |
XM_011529090.2 | 1823 | Missense Mutation | CCC,TCC | P,S 628 | XP_011527392.1 | |
XM_011529091.2 | 1823 | Missense Mutation | CCC,TCC | P,S 572 | XP_011527393.1 | |
XM_017028110.1 | 1823 | Missense Mutation | CCC,TCC | P,S 561 | XP_016883599.1 | |
XM_017028111.1 | 1823 | Missense Mutation | CCC,TCC | P,S 547 | XP_016883600.1 | |
XM_017028112.1 | 1823 | Missense Mutation | CCC,TCC | P,S 491 | XP_016883601.1 |