Product Details

SNP ID

rs117226808

Assay Type

Functionally tested

NCBI dbSNP Submissions

NA

Location

Chr.8:31040621 on Build GRCh38

Set Membership

Context Sequence [VIC/FAM]

TGCCGGTACATTGACTCAGATGAGC[A/G]TTGAGAATTGGCTATAGGATTTGAC

Phenotype

MIM: 604611

Polymorphism

A/G, Transition substitution

Allele Nomenclature

Literature Links

PURG PubMed Links

Gene Details

Gene

PURG

Gene Name

purine rich element binding protein G

There are no transcripts associated with this gene.

Gene

WRN

Gene Name

Werner syndrome RecQ like helicase

Transcript Accession	SNP Location	SNP Type	Codon Change	Amino Acid Change	Protein ID
NM_000553.4		Intron			NP_000544.2
XM_011544639.2		Intron			XP_011542941.1
XM_011544640.1		Intron			XP_011542942.1

View Full Product Details