ABCB4 c.355T>G ;(p.Y119D)

Variant ID: 7-87082441-A-C

NM_000443.3(ABCB4):c.355T>G;(p.Y119D)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Analysis of transcript-deleterious variants in Mendelian disorders: implications for RNA-based diagnostics.

Genome Biology
Maddirevula, Sateesh S; Kuwahara, Hiroyuki H; Ewida, Nour N; Shamseldin, Hanan E HE; Patel, Nisha N; Alzahrani, Fatema F; AlSheddi, Tarfa T; AlObeid, Eman E; Alenazi, Mona M; Alsaif, Hessa S HS; Alqahtani, Maha M; AlAli, Maha M; Al Ali, Hatoon H; Helaby, Rana R; Ibrahim, Niema N; Abdulwahab, Firdous F; Hashem, Mais M; Hanna, Nadine N; Monies, Dorota D; Derar, Nada N; Alsagheir, Afaf A; Alhashem, Amal A; Alsaleem, Badr B; Alhebbi, Hamoud H; Wali, Sami S; Umarov, Ramzan R; Gao, Xin X; Alkuraya, Fowzan S FS
Publication Date: 2020-06-17

Variant appearance in text: ABCB4: 355T>G; Tyr119Asp
PubMed Link: 32552793
Variant Present in the following documents:
  • Main text
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