Product Details

SNP ID: rs150070913
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:102937375 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: ACGACTTCCTGCTCAAGTTCCTGCT[G/T]GTGGGCGACAGGGACGTAGGCAAGA
Phenotype: MIM: 300405
Polymorphism: G/T, Transversion substitution
Allele Nomenclature
Literature Links: RAB40AL PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001031834.1	104	Silent Mutation	CTG,CTT	L19L	NP_001027004.1