Product Details

SNP ID
rs112921476
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:39605268 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GTTTCCGAGTGCACTTTGGCAATCA[C/T]GTGGTCATGAACAGGCGTGAGTTTG
Phenotype
MIM: 608717
Polymorphism
C/T, Transition substitution
Allele Nomenclature
Literature Links
LGALS13 PubMed Links

Gene Details

Gene
LGALS13
Gene Name
galectin 13
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_013268.2 223 Silent Mutation CAC,CAT H61H NP_037400.1
XM_011526874.2 223 Missense Mutation CAC,CAT H54H XP_011525176.1
XM_017026715.1 223 Missense Mutation CAC,CAT H92H XP_016882204.1

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