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SI c.4445T>C ;(p.I1482T)
Variant ID: 3-164716423-A-G
NM_001041.3(
SI
):c.4445T>C;(p.I1482T)
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:
Significance of rare variants in genes involved in the pathogenesis of Lynch syndrome.
International Journal Of Molecular Medicine
Liccardo, Raffaella R; Lambiase, Matilde M; Nolano, Antonio A; De Rosa, Marina M; Izzo, Paola P; Duraturo, Francesca F
Publication Date: 2022-06
Variant appearance in text: SI: 4445T>C; Ile1482Thr
PubMed Link:
35475445
Variant Present in the following documents:
ijmm-49-06-05137.pdf
View BVdb publication page