Product Details

SNP ID

rs145731782

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:172659310 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

AGTTCTTCCCTGTCCAACCTCTGTG[C/G]CCAGAAGGCCTGGTCAAAGGAGGCC

Phenotype

MIM: 134638

Polymorphism

C/G, Transversion 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	303	Missense Mutation	CCC,GCC	P37A	NP_000630.1
NM_001302746.1	303	Missense Mutation	CCC,GCC	P37A	NP_001289675.1

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