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ERBB2 c.1457T>C ;(p.F486S)
Variant ID: 17-37872136-T-C
NM_004448.2(
ERBB2
):c.1457T>C;(p.F486S)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
Google
UCSC Genome Browser
ClinVar
dbSNP
Publications:
Systematic review and meta-analysis of genomic alterations in acral melanoma.
Pigment Cell & Melanoma Research
Broit, Natasa N; Johansson, Peter A PA; Rodgers, Chloe B CB; Walpole, Sebastian T ST; Hayward, Nicholas K NK; Pritchard, Antonia L AL
Publication Date: 2022-05
Variant appearance in text: ERBB2: F486S
PubMed Link:
35229492
Variant Present in the following documents:
PCMR-35-369-s003.xlsx, sheet 12
View BVdb publication page
Assessment of coding region variants in Kuwaiti population: implications for medical genetics and population genomics.
Scientific Reports
John, Sumi Elsa SE; Antony, Dinu D; Eaaswarkhanth, Muthukrishnan M; Hebbar, Prashantha P; Channanath, Arshad Mohamed AM; Thomas, Daisy D; Devarajan, Sriraman S; Tuomilehto, Jaakko J; Al-Mulla, Fahd F; Alsmadi, Osama O; Thanaraj, Thangavel Alphonse TA
Publication Date: 2018-11-08
Variant appearance in text: ERBB2: 1457T>C
PubMed Link:
30409984
Variant Present in the following documents:
Main text
41598_2018_Article_34815.pdf
View BVdb publication page