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FLT4 c.1258+6_1258+10del
Variant ID: 5-180053100-CCCTGA-C
NM_182925.4(
FLT4
):c.1258+6_1258+10del
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:
FLT4 Mutations Are Associated with Segmental Lymphatic Dysfunction and Initial Lymphatic Aplasia in Patients with Milroy Disease.
Genes
Liu, Ningfei N; Gao, Minzhe M
Publication Date: 2021-10-13
Variant appearance in text: FLT4: 1258+6_1258+10del
PubMed Link:
34681005
Variant Present in the following documents:
Main text
genes-12-01611.pdf
View BVdb publication page