Product Details

SNP ID

rs199708789

Assay Type

Functionally tested

NCBI dbSNP Submissions

4

Location

Chr.1:181089161 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GCCACCCGCCGGCTGGGGAGAGCCG[C/T]CCCCGCCCGCCGCTCGTGCCTCTTG

Phenotype

MIM: 607177

Polymorphism

C/T, Transition substitution

Allele Nomenclature

Literature Links

IER5 PubMed Links

Gene Details

Gene

IER5

Gene Name

immediate early response 5

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_016545.4	660	Missense Mutation	CCC,TCC	P87S	NP_057629.2

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