Product Details

SNP ID
rs12810443
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.12:94149219 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
AGCCTCTCGCGCCTGTACCGGGACC[A/G]AGCGGGCAACTGCACAGAGCCGGTC
Phenotype
MIM: 604259
Polymorphism
A/G, Transition 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_005761.2 524 Missense Mutation CAA,CGA Q83R NP_005752.1
XM_006719186.3 524 Missense Mutation CAA,CGA Q83R XP_006719249.1
XM_011537730.2 524 Missense Mutation CAA,CGA Q83R XP_011536032.1
XM_011537731.2 524 Missense Mutation CAA,CGA Q83R XP_011536033.1
XM_017018671.1 524 Missense Mutation CAA,CGA Q83R XP_016874160.1
XM_017018672.1 524 Missense Mutation CAA,CGA Q83R XP_016874161.1

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