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NF1 c.3664C>T ;(p.P1222S)
Variant ID: 17-29560187-C-T
NM_001042492.2(
NF1
):c.3664C>T;(p.P1222S)
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:
Origins of myelodysplastic syndromes after aplastic anemia.
Blood
Negoro, Eiju E; Nagata, Yasunobu Y; Clemente, Michael J MJ; Hosono, Naoko N; Shen, Wenyi W; Nazha, Aziz A; Yoshizato, Tetsuichi T; Hirsch, Cassandra C; Przychodzen, Bartlomiej B; Mahfouz, Reda Z RZ; Kuzmanovic, Teodora T; Sekeres, Mikkael A MA; Makishima, Hideki H; Ogawa, Seishi S; Maciejewski, Jaroslaw P JP
Publication Date: 2017-10-26
Variant appearance in text: NF1: P1222S
PubMed Link:
28893734
Variant Present in the following documents:
Main text
View BVdb publication page