Product Details

SNP ID

hCV89423233

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:39709262 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GATTCCCGCCAGCATCTGTGAAGAT[C/G]CTGCAAGTCTTCAGAGATATCTCCC

Phenotype

MIM: 607260

Polymorphism

C/G, Transversion substitution

Allele Nomenclature

Literature Links

LGALS14 PubMed Links

Gene Details

Gene

LGALS14

Gene Name

galectin 14

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020129.2	592	Missense Mutation	ATC,ATG	I123M	NP_064514.1
NM_203471.1	592	Missense Mutation	ATC,ATG	I152M	NP_982297.1

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