Product Details

SNP ID
rs150634780
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48405765 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TTGATGTACTTGTAGAGTTCATGCA[A/G]GGCCACTCGCGCCCCGAGGTCTCCG
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 9950 Silent Mutation CTG,TTG L2088L NP_001123554.1
NM_002673.5 9950 Silent Mutation CTG,TTG L2088L NP_002664.2
XM_011533833.2 9950 Silent Mutation CTG,TTG L2089L XP_011532135.1
XM_011533834.1 9950 Silent Mutation CTG,TTG L2089L XP_011532136.1
XM_011533835.1 9950 Silent Mutation CTG,TTG L2089L XP_011532137.1
XM_011533836.1 9950 Silent Mutation CTG,TTG L2089L XP_011532138.1
XM_011533837.2 9950 Silent Mutation CTG,TTG L2089L XP_011532139.1
XM_017006630.1 9950 Silent Mutation CTG,TTG L2089L XP_016862119.1
XM_017006631.1 9950 Silent Mutation CTG,TTG L2088L XP_016862120.1

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