Product Details

SNP ID
rs144549146
Assay Type
Functionally Tested
NCBI dbSNP Submissions
NA
Location
Chr.19:51125138 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]
TCGCATGGCTGGATTTACCCTGGCC[C/T]AGTAGTTCATGGCTACTGGTTCCGG
Phenotype
MIM: 605640
Polymorphism
C/T, Transition Substitution
Allele Nomenclature
Literature Links
SIGLEC9 PubMed Links

Gene Details

Gene
SIGLEC9
Gene Name
sialic acid binding Ig like lectin 9
Transcript Accession SNP Location SNP Type Codon Change Amino Acid Change Protein ID
NM_001198558.1 231 Missense Mutation CCA,CTA P55L NP_001185487.1
NM_014441.2 231 Missense Mutation CCA,CTA P55L NP_055256.1
XM_006723146.3 231 Missense Mutation CCA,CTA P55L XP_006723209.1
XM_011526730.2 231 Missense Mutation CCA,CTA P55L XP_011525032.1
XM_011526732.2 231 Missense Mutation CCA,CTA P55L XP_011525034.1
XM_017026595.1 231 Missense Mutation CCA,CTA P55L XP_016882084.1
XM_017026596.1 231 Missense Mutation CCA,CTA P55L XP_016882085.1

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