Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
GTTTGCACTTGAGCATCCAACATCC[A/G]CTTTGGTCCCTGGAGAAAAACAGAA
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) - Not Available | |||
EAS
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African American - Not Available | YRI (Yoruba) - Not Available | |||
SAS
|
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
|
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 | 1766 | Missense Mutation | CGG,TGG | R,W 486 | NP_001303290.1 | |
NM_001323347.1 | 1766 | Missense Mutation | CGG,TGG | R,W 486 | NP_001310276.1 | |
NM_003657.3 | 1766 | Missense Mutation | CGG,TGG | R,W 564 | NP_003648.2 | |
XM_005260587.2 | 1766 | Missense Mutation | CGG,TGG | R,W 609 | XP_005260644.1 | |
XM_005260589.2 | 1766 | Missense Mutation | CGG,TGG | R,W 595 | XP_005260646.1 | |
XM_005260590.2 | 1766 | Missense Mutation | CGG,TGG | R,W 587 | XP_005260647.1 | |
XM_005260591.2 | 1766 | Missense Mutation | CGG,TGG | R,W 573 | XP_005260648.1 | |
XM_005260593.2 | 1766 | Missense Mutation | CGG,TGG | R,W 550 | XP_005260650.1 | |
XM_005260594.2 | 1766 | Missense Mutation | CGG,TGG | R,W 531 | XP_005260651.1 | |
XM_005260595.2 | 1766 | Missense Mutation | CGG,TGG | R,W 517 | XP_005260652.1 | |
XM_011529090.2 | 1766 | Missense Mutation | CGG,TGG | R,W 609 | XP_011527392.1 | |
XM_011529091.2 | 1766 | Missense Mutation | CGG,TGG | R,W 553 | XP_011527393.1 | |
XM_017028110.1 | 1766 | Missense Mutation | CGG,TGG | R,W 542 | XP_016883599.1 | |
XM_017028111.1 | 1766 | Missense Mutation | CGG,TGG | R,W 528 | XP_016883600.1 | |
XM_017028112.1 | 1766 | Missense Mutation | CGG,TGG | R,W 472 | XP_016883601.1 |