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MTHFR c.177G>C ;(p.W59C)
Variant ID: 1-11862997-C-G
NM_005957.4(
MTHFR
):c.177G>C;(p.W59C)
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:
A Glance into MTHFR Deficiency at a Molecular Level.
International Journal Of Molecular Sciences
Savojardo, Castrense C; Babbi, Giulia G; Baldazzi, Davide D; Martelli, Pier Luigi PL; Casadio, Rita R
Publication Date: 2021-12-23
Variant appearance in text: MTHFR: W59C
PubMed Link:
35008593
Variant Present in the following documents:
Main text
ijms-23-00167.pdf
View BVdb publication page
A Glance into MTHFR Deficiency at a Molecular Level.
International Journal Of Molecular Sciences
Savojardo, Castrense C; Babbi, Giulia G; Baldazzi, Davide D; Martelli, Pier Luigi PL; Casadio, Rita R
Publication Date: 2021-12-23
Variant appearance in text: MTHFR: W59C
PubMed Link:
35008593
Variant Present in the following documents:
Main text
ijms-23-00167.pdf
View BVdb publication page