Product Details

SNP ID

rs139357251

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.19:57958633 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

GTCTTCCATTTTTCCATTATGTGAC[A/G]CATTCTTTGTTTTGTTTTCTGTTAC

Phenotype

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

C19orf18 PubMed Links

Gene Details

Gene

C19orf18

Gene Name

chromosome 19 open reading frame 18

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_152474.4	719	Missense Mutation	GCG,GTG	A206V	NP_689687.1

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