Product Details

SNP ID: rs4698603
Assay Type: Functionally tested
NCBI dbSNP Submissions: NA
Location: Chr.4:17518244 on Build GRCh38
Set Membership: HapMap
Context Sequence [VIC/FAM]: AATAAATTCCCACGCCAATCATGGA[A/G]AAAACCAAAGAACTATCCATCGCAA
Phenotype: MIM: 612676
Polymorphism: A/G, Transition substitution
Allele Nomenclature
Literature Links: CLRN2 PubMed Links

Gene Details

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_001079827.2		Intron			NP_001073296.1

There are no transcripts associated with this gene.