ULK4 c.889_891del ;(p.S297del)

Variant ID: 3-41954304-GACT-G

NM_017886.2(ULK4):c.889_891del;(p.S297del)

This variant was identified in 1 publication

View GRCh38 version.




Publications:


Exome sequencing reveals variants in known and novel candidate genes for severe sperm motility disorders.

Human Reproduction (Oxford, England)
Oud, M S MS; Houston, B J BJ; Volozonoka, L L; Mastrorosa, F K FK; Holt, G S GS; Alobaidi, B K S BKS; deVries, P F PF; Astuti, G G; Ramos, L L; Mclachlan, R I RI; O'Bryan, M K MK; Veltman, J A JA; Chemes, H E HE; Sheth, H H
Publication Date: 2021-08-18

Variant appearance in text: ULK4: s297delins
PubMed Link: 34089056
Variant Present in the following documents:
  • deab099_supplementary_tables3.pdf
View BVdb publication page