Product Details

SNP ID: rs61757468
Assay Type: Functionally tested
NCBI dbSNP Submissions: 8
Location: Chr.1:119894118 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: AGTTTTTGTTTTAGATTCTTCCTGT[A/C]CAGTTTTTGTTTTAGATTCTTCCTG
Phenotype: MIM: 604779
Polymorphism: A/C, Transversion substitution
Allele Nomenclature
Literature Links: ADAM30 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_021794.3	2407	Missense Mutation			NP_068566.2