Product Details

SNP ID

rs199998646

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.11:17367278 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGGGACTGTCTACCAGTGTGTGGTA[C/T]GGCATGCGTCCTTGCATACCCCCTT

Phenotype

MIM: 613714

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

NCR3LG1 PubMed Links

Gene Details

Gene

NCR3LG1

Gene Name

natural killer cell cytotoxicity receptor 3 ligand 1

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001202439.2	2505	Missense Mutation	CGG,TGG	R231W	NP_001189368.1
XM_011520072.2	2505	Missense Mutation	CGG,TGG	R202W	XP_011518374.1
XM_011520073.2	2505	Missense Mutation	CGG,TGG	R202W	XP_011518375.1
XM_011520074.2	2505	Missense Mutation	CGG,TGG	R202W	XP_011518376.1
XM_011520075.2	2505	Missense Mutation	CGG,TGG	R202W	XP_011518377.1

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