Early embryonic failure caused by a novel mutation in the TUBB8 gene: A case report

Table 2 Results of sequencing mutation sites in the coding region of the TUBB8 gene in the patient (female)

Gene	Chromosomal location	Variant naming	Frequency	Zygotic type	Source of variation
TUBB8	Chr 93730	NM_177987.3: c.602G>T(p.C201F)	Not included	Heterozygous	Unknown

Remarks: The variation verification result may be the complementary sequence of the reference sequence, and the variation C>A can also be expressed as G>T.