Product Details

SNP ID
rs189131085
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:74697297 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
CTTGATCTGAGTCAAGTGGAAGATT[A/C]CTGAGGGCAGAGACAAGGATGTGAG
Phenotype
MIM: 613127
Polymorphism
A/C, Transversion substitution
Allele Nomenclature
Literature Links
CHRDL2 PubMed Links

Gene Details

Gene
CHRDL2
Gene Name
chordin like 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001278473.2 1315 Missense Mutation NP_001265402.1
NM_001304390.1 1315 Silent Mutation NP_001291319.1
NM_001304391.1 1315 Silent Mutation NP_001291320.1
NM_001304415.1 1315 Missense Mutation NP_001291344.1
NM_001304416.1 1315 Missense Mutation NP_001291345.1
NM_001304417.1 1315 Silent Mutation NP_001291346.1
NM_015424.5 1315 Silent Mutation NP_056239.3

View Full Product Details