KIT c.1502C>T ;(p.S501F)

KIT c.1502C>T ;(p.S501F)

Variant ID: 4-55592178-C-T

NM_000222.2(KIT):c.1502C>T;(p.S501F)

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:

Mutational concordance between primary and metastatic melanoma: a next-generation sequencing approach.

Journal Of Translational Medicine

Manca, Antonella A; Paliogiannis, Panagiotis P; Colombino, Maria M; Casula, Milena M; Lissia, Amelia A; Botti, Gerardo G; Caracò, Corrado C; Ascierto, Paolo A PA; Sini, Maria Cristina MC; Palomba, Grazia G; Pisano, Marina M; , ; , ; Doneddu, Valentina V; Cossu, Antonio A; Palmieri, Giuseppe G; ,

Publication Date: 2019-08-28

Variant appearance in text: KIT: 1502C>T; Ser501Phe

PubMed Link: 31455347

Variant Present in the following documents:

12967_2019_2039_MOESM1_ESM.xlsx, sheet 1

View BVdb publication page