Product Details

SNP ID: rs144436978
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:71119535 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTGGAAGAATCTAAGAAGGAGCAAA[C/G]GCCCTGGGTTGGGAAGACTTATAGG
Phenotype: MIM: 308380 MIM: 300188
Polymorphism: C/G, Transversion substitution
Allele Nomenclature
Literature Links: IL2RG PubMed Links

Gene Details

There are no transcripts associated with this gene.

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_005120.2		Intron			NP_005111.2