Product Details

SNP ID

rs1065442

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.2:203870748 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GAAGTCTGTGCGGCAACCTACATGA[C/T]GGGGAATGAGTTGACCTTCCTAGAT

Phenotype

MIM: 123890

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

CTLA4 PubMed Links

Gene Details

Gene

CTLA4

Gene Name

cytotoxic T-lymphocyte associated protein 4

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001037631.2	427	Missense Mutation	ACG,ATG	T91M	NP_001032720.1
NM_005214.4	427	Missense Mutation	ACG,ATG	T91M	NP_005205.2

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