Product Details

SNP ID
rs185819379
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.8:66566924 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGGTTCATCTTCCTCTTTGAGGAA[C/T]AGGTCTGTTCCAGTTTCTTCTTTTA
Phenotype
MIM: 159405
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
MYBL1 PubMed Links

Gene Details

Gene
MYBL1
Gene Name
MYB proto-oncogene like 1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001080416.3 2072 Silent Mutation NP_001073885.1
NM_001144755.2 2072 Silent Mutation NP_001138227.1
NM_001294282.1 2072 Silent Mutation NP_001281211.1
XM_011517533.2 2072 Silent Mutation XP_011515835.1
XM_011517535.2 2072 Silent Mutation XP_011515837.1
XM_017013455.1 2072 Silent Mutation XP_016868944.1
XM_017013456.1 2072 Silent Mutation XP_016868945.1
XM_017013457.1 2072 Silent Mutation XP_016868946.1
XM_017013458.1 2072 Silent Mutation XP_016868947.1
XM_017013459.1 2072 Intron XP_016868948.1

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