Product Details

SNP ID
rs199944599
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.7:73539926 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CAGCGTTGGGGGCTGGGAGTCATCC[A/G]TGCGGAAGTCGGAGGTGTGTGCTGG
Phenotype
MIM: 605846
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
BCL7B PubMed Links

Gene Details

Gene
BCL7B
Gene Name
BCL tumor suppressor 7B
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001197244.1 549 Intron NP_001184173.1
NM_001301061.1 549 Missense Mutation ACG,ATG T142M NP_001287990.1
NM_001707.3 549 Missense Mutation ACG,ATG T131M NP_001698.2

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