Product Details

SNP ID: rs186774716
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:136648337 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AAAATTTTTATGTATTTACTTACTG[C/T]TTTTCTTATCACCCAGATGATTGGG
Phenotype: MIM: 300386
Polymorphism: C/T, Transition substitution
Allele Nomenclature
Literature Links: CD40LG PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000074.2	161	Missense Mutation	GCT,GTT	A30V	NP_000065.1

There are no transcripts associated with this gene.