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TTTTTAGTAAGTGTATATGTTTTGT[C/T]GGTTGAATTTATATCTTGTTTTTCA
Species: |
Human | ||||||||||||||||||||
dbSNP Submissions: |
NA
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Phenotype: |
MIM: 159405 | ||||||||||||||||||||
Literature Links: |
MYBL1 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 |
MYBL1 - MYB proto-oncogene like 1 | ||||||
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Transcript Accession | SNP Location | SNP Type | Observed Codons | Observed Amino Acid | Protein ID | |
NM_001080416.3 | 2464 | Missense Mutation | AAC,GAC | N,D 685 | NP_001073885.1 | |
NM_001144755.2 | 2464 | Intron | NP_001138227.1 | |||
NM_001294282.1 | 2464 | Intron | NP_001281211.1 | |||
XM_011517533.2 | 2464 | Missense Mutation | AAC,GAC | N,D 690 | XP_011515835.1 | |
XM_011517535.2 | 2464 | Intron | XP_011515837.1 | |||
XM_017013455.1 | 2464 | Missense Mutation | AAC,GAC | N,D 703 | XP_016868944.1 | |
XM_017013456.1 | 2464 | Missense Mutation | AAC,GAC | N,D 698 | XP_016868945.1 | |
XM_017013457.1 | 2464 | Intron | XP_016868946.1 | |||
XM_017013458.1 | 2464 | Intron | XP_016868947.1 | |||
XM_017013459.1 | 2464 | Intron | XP_016868948.1 |