Product Details

SNP ID: rs201801746
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.20:25248240 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CAGATCAGCGTGCGCGGCCTGGCGG[A/G]GCTAGGCGACGTGGCCGAGGTGCGG
Phenotype: MIM: 138550
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: LOC105372580 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_002862.3	171	Missense Mutation	GAG,GGG	E21G	NP_002853.2