Product Details

SNP ID: rs76169344
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.2:8731378 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CTCAGCACTGTGTTCTGGAGACTTC[A/G]GCACTCTCTCTACTTTCCCTTCGGC
Phenotype: MIM: 615759
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: KIDINS220 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_020738.2	4840	Missense Mutation			NP_065789.1