"GeneDx"[submitter] AND "UNG"[gene] - ClinVar

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Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 145881	GRCh38/hg38 12q24.11(chr12:109081325-109154941)x3	ACACB, ALKBH2 +4 more	Copy number gain	See cases	GLikely benign
Select item 1244809	NM_080911.3(UNG):c.132+193A>G	LOC130008712, UNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1258409	NM_080911.3(UNG):c.132+241T>A	LOC130008712, UNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251149	NM_080911.3(UNG):c.133-221C>T	UNG	Single nucleotide variant (5 prime UTR variant +1 more)	not provided	GBenign
Select item 440391	NM_080911.3(UNG):c.262C>T (p.Arg88Cys)	UNG (R88C +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 3363490	NM_080911.3(UNG):c.313G>T (p.Glu105Ter)	UNG (E105* +1 more)	Single nucleotide variant (nonsense)	not provided	GUncertain significance
Select item 2507339	NM_080911.3(UNG):c.339G>T (p.Lys113Asn)	UNG (K104N +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1260707	NM_080911.3(UNG):c.339+116A>C	UNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249431	NM_080911.3(UNG):c.534-25dup	UNG	Duplication (intron variant)	not provided +1 more	GBenign
Select item 1244513	NM_080911.3(UNG):c.622+42dup	UNG	Duplication (intron variant)	not provided	GBenign
Select item 1230454	NM_080911.3(UNG):c.623-67T>C	UNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 306978	NM_080911.3(UNG):c.769T>C (p.Tyr257His)	UNG (Y257H +1 more)	Single nucleotide variant (missense variant)	Hyper-IgM syndrome type 5 +2 more	GUncertain significance
Select item 1308769	NM_080911.3(UNG):c.799dup (p.Arg267fs)	UNG (R258fs +1 more)	Duplication (frameshift variant)	not provided	GUncertain significance
Select item 2662425	NM_080911.3(UNG):c.802-51_802-48dup	UNG	Duplication (intron variant)	not provided	GLikely benign
Select item 1221105	NM_080911.3(UNG):c.802-53_802-48dup	UNG	Duplication (intron variant)	not provided	GBenign
Select item 1707290	NM_080911.3(UNG):c.802-48del	UNG	Deletion (intron variant)	not provided	GLikely benign
Select item 1289653	NM_080911.3(UNG):c.802-48_802-47insAAAT	UNG	Insertion (intron variant)	not provided	GBenign
Select item 1271811	NM_080911.3(UNG):c.802-48_802-47insAAT	UNG	Insertion (intron variant)	not provided	GBenign
Select item 1264165	NM_080911.3(UNG):c.802-48_802-47insAAAAT	UNG	Insertion (intron variant)	not provided	GBenign
Select item 1229315	NM_080911.3(UNG):c.802-48A>T	UNG	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231991	NM_080911.3(UNG):c.802-47T>A	UNG	Single nucleotide variant (intron variant)	not provided	GBenign

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Items: 21