Product Details

SNP ID
rs139734110
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.11:74696513 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCTGCAACTGTTAGGTCTTTGTTAT[A/G]TCTTGGTCACTTTGTCTGGACTGGC
Phenotype
MIM: 613127
Polymorphism
A/G, Transition 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 1480 Missense Mutation ACA,ATA T429I NP_001265402.1
NM_001304390.1 1480 Silent Mutation GAC,GAT D427D NP_001291319.1
NM_001304391.1 1480 Silent Mutation GAC,GAT D362D NP_001291320.1
NM_001304415.1 1480 Missense Mutation ACA,ATA T344I NP_001291344.1
NM_001304416.1 1480 Missense Mutation ACA,ATA T313I NP_001291345.1
NM_001304417.1 1480 Silent Mutation GAC,GAT D382D NP_001291346.1
NM_015424.5 1480 Silent Mutation GAC,GAT D447D NP_056239.3

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