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MTHFR c.604_624del ;(p.P202_E208del)
Variant ID: 1-11856419-CCTCAAAGCTCCCTGCTTCGGG-C
NM_005957.4(
MTHFR
):c.604_624del;(p.P202_E208del)
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:
Genetic Testing in Various Neurodevelopmental Disorders Which Manifest as Cerebral Palsy: A Case Study From Iran.
Frontiers In Pediatrics
Nejabat, Marzieh M; Inaloo, Soroor S; Sheshdeh, Afsaneh Taghipour AT; Bahramjahan, Shima S; Sarvestani, Fatima Masoomi FM; Katibeh, Pegah P; Nemati, Hamid H; Tabei, Seyed Mohammad Bagher SMB; Faghihi, Mohammad Ali MA
Publication Date: 2021
Variant appearance in text: MTHFR: 604_624del
PubMed Link:
34540776
Variant Present in the following documents:
Main text
fped-09-734946.pdf
View BVdb publication page