"Fulgent Genetics, Fulgent Genetics"[submitter] AND "LOC130055524"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 456276	NM_020937.4(FANCM):c.53G>A (p.Arg18Gln)	FANCM, LOC130055524 (R18Q)	Single nucleotide variant (missense variant)	Fanconi anemia complementation group A +5 more	GConflicting classifications of pathogenicity
Select item 841002	NM_020937.4(FANCM):c.56C>T (p.Ser19Leu)	FANCM, LOC130055524 (S19L)	Single nucleotide variant (missense variant)	Fanconi anemia +3 more	GUncertain significance
Select item 861897	NM_020937.4(FANCM):c.71G>T (p.Gly24Val)	FANCM, LOC130055524 (G24V)	Single nucleotide variant (missense variant)	Spermatogenic failure 28 +2 more	GUncertain significance
Select item 1122592	NM_020937.4(FANCM):c.81C>T (p.Ser27=)	FANCM, LOC130055524	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GLikely benign
Select item 841311	NM_020937.4(FANCM):c.83G>T (p.Gly28Val)	FANCM, LOC130055524 (G28V)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 456281	NM_020937.4(FANCM):c.88G>C (p.Glu30Gln)	FANCM, LOC130055524 (E30Q)	Single nucleotide variant (missense variant)	Fanconi anemia +2 more	GUncertain significance
Select item 702243	NM_020937.4(FANCM):c.93A>G (p.Arg31=)	FANCM, LOC130055524	Single nucleotide variant (synonymous variant)	Fanconi anemia +2 more	GLikely benign

ClinVar