Product Details

SNP ID: rs201893153
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.X:70259032 on Build GRCh38
Set Membership
Context Sequence [VIC/FAM]: CCCCATGACCGCCGAGCTGAAGTGC[A/G]CATAGTGGTCAAACTCTTCAGGCCG
Phenotype: MIM: 301770 MIM: 300038
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: ARR3 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_002565.3	773	Missense Mutation	GCG,GTG	A198V	NP_002556.1