Product Details

SNP ID
rs150572663
Assay Type
Functionally tested
NCBI dbSNP Submissions
NA
Location
Chr.19:39605285 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
GGCAATCATGTGGTCATGAACAGGC[A/G]TGAGTTTGGGATATGGATGTTGGAG
Phenotype
MIM: 608717
Polymorphism
A/G, 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_013268.2 240 Missense Mutation CAT,CGT H67R NP_037400.1
XM_011526874.2 240 Missense Mutation CAT,CGT H60R XP_011525176.1
XM_017026715.1 240 Missense Mutation CAT,CGT H98R XP_016882204.1

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