Related gene-specific medical variations for Gene (Select 134492) - ClinVar - NCBI

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Items: 10

	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 3202746	NM_145266.6(NUDCD2):c.184C>T (p.Leu62Phe)	LOC129995199, NUDCD2 (L62F)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3202745	NM_145266.6(NUDCD2):c.148C>G (p.Arg50Gly)	LOC129995199, NUDCD2 (R50G)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 3202744	NM_145266.6(NUDCD2):c.139C>T (p.Leu47Phe)	LOC129995199, NUDCD2 (L47F)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2562204	NM_145266.6(NUDCD2):c.31G>A (p.Val11Met)	LOC129995199, NUDCD2 (V11M)	Single nucleotide variant (5 prime UTR variant +2 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 2512989	NM_145266.6(NUDCD2):c.149G>A (p.Arg50Gln)	LOC129995199, NUDCD2 (R50Q)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2407691	NM_145266.6(NUDCD2):c.252G>A (p.Met84Ile)	NUDCD2, CCNG1 (M84I +1 more)	Single nucleotide variant (missense variant +1 more)	Inborn genetic diseases	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 2380567	NM_145266.6(NUDCD2):c.29G>A (p.Gly10Glu)	LOC129995199, NUDCD2 (G10E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance