Product Details

SNP ID
rs34781337
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.3:48406876 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
ATCTCTTGGTCGCTGGCTGGGACAG[A/T]CTGTCTGATGTCTGCATAGTACCTG
Phenotype
MIM: 601053
Polymorphism
A/T, Transversion 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 9863 Missense Mutation ACT,TCT T2059S NP_001123554.1
NM_002673.5 9863 Missense Mutation ACT,TCT T2059S NP_002664.2
XM_011533833.2 9863 Missense Mutation ACT,TCT T2060S XP_011532135.1
XM_011533834.1 9863 Missense Mutation ACT,TCT T2060S XP_011532136.1
XM_011533835.1 9863 Missense Mutation ACT,TCT T2060S XP_011532137.1
XM_011533836.1 9863 Missense Mutation ACT,TCT T2060S XP_011532138.1
XM_011533837.2 9863 Missense Mutation ACT,TCT T2060S XP_011532139.1
XM_017006630.1 9863 Missense Mutation ACT,TCT T2060S XP_016862119.1
XM_017006631.1 9863 Missense Mutation ACT,TCT T2059S XP_016862120.1

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