NOTCH1 c.2953C>G ;(p.P985A)

Variant ID: 9-139404201-G-C

NM_017617.3(NOTCH1):c.2953C>G;(p.P985A)

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 analysis of products of conception identifies novel mutations associated with missed abortion.

Molecular Medicine Reports
Fu, Meng M; Mu, Sha S; Wen, Chunyan C; Jiang, Shufang S; Li, Lin L; Meng, Yuanguang Y; Peng, Hongmei H
Publication Date: 2018-08

Variant appearance in text: NOTCH1: 2953C>G; P985A
PubMed Link: 29956774
Variant Present in the following documents:
  • Main text
  • mmr-18-02-2027.pdf
View BVdb publication page