Related gene-specific medical variations for Gene (Select 900) - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3202747	NM_145266.6(NUDCD2):c.436A>G (p.Thr146Ala)	CCNG1, NUDCD2 (T146A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539865	NM_145266.6(NUDCD2):c.467A>C (p.Glu156Ala)	CCNG1, NUDCD2 (E156A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2407691	NM_145266.6(NUDCD2):c.252G>A (p.Met84Ile)	CCNG1, NUDCD2 (M84I +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2391267	NM_145266.6(NUDCD2):c.310C>G (p.Leu104Val)	CCNG1, NUDCD2 (L104V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 563121	GRCh37/hg19 5q34(chr5:162772647-162878762)x1	CCNG1	Copy number loss	not provided	GUncertain significance

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