Search Thermo Fisher Scientific
Search Thermo Fisher Scientific
CTCGTCGGTCTCCGAGGATGGAGAT[A/G]GCTCAGGTGCGCGACCCACTGCTGG
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
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Literature Links: |
BRMS1L 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 |
BRMS1L - breast cancer metastasis-suppressor 1-like | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_032352.3 | 1057 | Missense Mutation | AGC,GGC | S,G 46 | NP_115728.2 | |
XM_005268128.1 | 1057 | Missense Mutation | AGC,GGC | S,G 46 | XP_005268185.1 | |
XM_006720274.2 | 1057 | UTR 5 | XP_006720337.1 | |||
XM_006720275.2 | 1057 | UTR 5 | XP_006720338.1 | |||
XM_017021703.1 | 1057 | Intron | XP_016877192.1 | |||
XM_017021704.1 | 1057 | Intron | XP_016877193.1 | |||
XM_017021705.1 | 1057 | Intron | XP_016877194.1 | |||
XM_017021706.1 | 1057 | Missense Mutation | AGC,GGC | S,G 156 | XP_016877195.1 |