Product Details

SNP ID: rs3827103
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:56248973 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: TGAGCAGGTCTTCATCAAGCCCGAG[A/G]TTTTCCTGTCTCTGGGCATCGTCAG
Phenotype: MIM: 155540
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: MC3R PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_019888.3	242	Missense Mutation	ATT,GTT	I44V	NP_063941.3