Product Details

SNP ID

rs200113302

Assay Type

Functionally tested

NCBI dbSNP Submissions

1

Location

Chr.1:172660114 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TACTAGTCTACCAGCCAGATGCACA[C/T]AGCATCATCTTTGGAGAAGCAAATA

Phenotype

MIM: 134638

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

FASLG PubMed Links

Gene Details

Gene

FASLG

Gene Name

Fas ligand

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000639.2	562	Missense Mutation	ACA,ATA	T123I	NP_000630.1
NM_001302746.1	562	Intron			NP_001289675.1

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