HERC2 c.2659C>A ;(p.Q887K)

Variant ID: 15-28501322-G-T

NM_004667.5(HERC2):c.2659C>A;(p.Q887K)

This variant was identified in 1 publication

View GRCh38 version.



Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP

Publications:

Whole-exome sequencing identifies a novel somatic mutation in MMP8 associated with a t(1;22)-acute megakaryoblastic leukemia.

Leukemia
Kim, Y Y; Schulz, V P VP; Satake, N N; Gruber, T A TA; Teixeira, A M AM; Halene, S S; Gallagher, P G PG; Krause, D S DS
Publication Date: 2014-04

Variant appearance in text: HERC2: Q887K
PubMed Link: 24157583
Variant Present in the following documents:
  • Main text
  • nihms549969.pdf
View BVdb publication page