Product Details

SNP ID

rs142659483

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39605284 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGCAATCATGTGGTCATGAACAGG[C/T]GTGAGTTTGGGATATGGATGTTGGA

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	239	Missense Mutation	CGT,TGT	R67C	NP_037400.1
XM_011526874.2	239	Missense Mutation	CGT,TGT	R60C	XP_011525176.1
XM_017026715.1	239	Missense Mutation	CGT,TGT	R98C	XP_016882204.1

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