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FBN1 c.4009G>C ;(p.A1337P)
Variant ID: 15-48766803-C-G
NM_000138.4(
FBN1
):c.4009G>C;(p.A1337P)
This variant was identified in 2 publications
View GRCh38 version.
Variant-Specific Resource Links:
gnomAD v2.1.1
Mutalizer Name Checker
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dbSNP
Publications:
Assembly assay identifies a critical region of human fibrillin-1 required for 10-12 nm diameter microfibril biogenesis.
Plos One
Jensen, Sacha A SA; Atwa, Ondine O; Handford, Penny A PA
Publication Date: 2021
Variant appearance in text: FBN1: A1337P
PubMed Link:
33735269
Variant Present in the following documents:
Main text
pone.0248532.s001.xlsx, sheet 1
pone.0248532.pdf
View BVdb publication page
Assessment of computational methods for predicting the effects of missense mutations in human cancers.
Bmc Genomics
Gnad, Florian F; Baucom, Albion A; Mukhyala, Kiran K; Manning, Gerard G; Zhang, Zemin Z
Publication Date: 2013
Variant appearance in text: FBN1: A1337P
PubMed Link:
23819521
Variant Present in the following documents:
1471-2164-14-S3-S7-S1.xlsx, sheet 2
View BVdb publication page