Product Details

SNP ID
rs200619004
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:94149750 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AACTACACGAGCGGCGCTGCCACCG[C/G]CTGGCCCAGCATGGCGCGCATCGCG
Phenotype
MIM: 604259
Polymorphism
C/G, Transversion substitution
Allele Nomenclature
Literature Links
PLXNC1 PubMed Links

Gene Details

Gene
PLXNC1
Gene Name
plexin C1
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_005761.2 1055 Missense Mutation GCC,GGC A260G NP_005752.1
XM_006719186.3 1055 Missense Mutation GCC,GGC A260G XP_006719249.1
XM_011537730.2 1055 Missense Mutation GCC,GGC A260G XP_011536032.1
XM_011537731.2 1055 Missense Mutation GCC,GGC A260G XP_011536033.1
XM_017018671.1 1055 Missense Mutation GCC,GGC A260G XP_016874160.1
XM_017018672.1 1055 Missense Mutation GCC,GGC A260G XP_016874161.1

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