Product Details

SNP ID
rs201622691
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.21:20998581 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCCTGAACATGAGCCTCCTCCTCTC[C/T]TTCTACCTGCTGGGGTTGCTTGTCA
Phenotype
MIM: 602040
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
NCAM2 PubMed Links

Gene Details

Gene
NCAM2
Gene Name
neural cell adhesion molecule 2
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_004540.3 130 Silent Mutation TCC,TCT S6S NP_004531.2
XM_011529575.2 130 Intron XP_011527877.1
XM_011529576.2 130 UTR 5 XP_011527878.1
XM_011529579.2 130 Silent Mutation TCC,TCT S6S XP_011527881.1
XM_011529580.2 130 Intron XP_011527882.1
XM_011529581.2 130 Intron XP_011527883.1
XM_011529582.2 130 Intron XP_011527884.1
XM_011529585.2 130 Intron XP_011527887.1
XM_017028353.1 130 UTR 5 XP_016883842.1
XM_017028354.1 130 Silent Mutation TCC,TCT S6S XP_016883843.1
XM_017028355.1 130 Silent Mutation TCC,TCT S6S XP_016883844.1
XM_017028356.1 130 UTR 5 XP_016883845.1
XM_017028357.1 130 UTR 5 XP_016883846.1
XM_017028358.1 130 Intron XP_016883847.1

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