Related gene-specific medical variations for Gene (Select 51314) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 810085	NM_016616.5(NME8):c.1012A>T (p.Ile338Phe)	NME8 (I338F)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 260766	NM_016616.5(NME8):c.621+48G>T	NME8	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 260765	NM_016616.5(NME8):c.594C>G (p.Val198=)	NME8	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 260763	NM_016616.5(NME8):c.528+46_528+48del	NME8	Microsatellite (intron variant)	not specified	GLikely benign
Select item 260757	NM_016616.5(NME8):c.1545-15C>T	NME8	Single nucleotide variant (intron variant)	not specified	GLikely benign
Select item 260752	NM_016616.5(NME8):c.-5G>T	NME8	Single nucleotide variant (5 prime UTR variant)	not specified	GLikely benign
Select item 241111	NM_016616.4(NME8):c.1400-?_*15+?dup	NME8	Duplication	Primary ciliary dyskinesia 6	GUncertain significance

ClinVar