Product Details

SNP ID
rs189943509
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48406831 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GCAGAGGGAGGCCTTACCCAGGACA[A/G]TTCAGCCAGGACAGAGTTCATCTCT
Phenotype
MIM: 601053
Polymorphism
A/G, Transition substitution
Allele Nomenclature
Literature Links
PLXNB1 PubMed Links

Gene Details

Gene
PLXNB1
Gene Name
plexin B1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001130082.2 9908 Silent Mutation CTG,TTG L2074L NP_001123554.1
NM_002673.5 9908 Silent Mutation CTG,TTG L2074L NP_002664.2
XM_011533833.2 9908 Silent Mutation CTG,TTG L2075L XP_011532135.1
XM_011533834.1 9908 Silent Mutation CTG,TTG L2075L XP_011532136.1
XM_011533835.1 9908 Silent Mutation CTG,TTG L2075L XP_011532137.1
XM_011533836.1 9908 Silent Mutation CTG,TTG L2075L XP_011532138.1
XM_011533837.2 9908 Silent Mutation CTG,TTG L2075L XP_011532139.1
XM_017006630.1 9908 Silent Mutation CTG,TTG L2075L XP_016862119.1
XM_017006631.1 9908 Silent Mutation CTG,TTG L2074L XP_016862120.1

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