"Fulgent Genetics, Fulgent Genetics"[submitter] AND "DNASE1L3"[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1355726	NM_004944.4(DNASE1L3):c.854G>A (p.Arg285Lys)	DNASE1L3 (R255K +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1484433	NM_004944.4(DNASE1L3):c.803C>G (p.Ala268Gly)	DNASE1L3 (A238G +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1652167	NM_004944.4(DNASE1L3):c.801+17G>C	DNASE1L3	Single nucleotide variant (intron variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GLikely benign
Select item 720102	NM_004944.4(DNASE1L3):c.777A>G (p.Lys259=)	DNASE1L3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1388385	NM_004944.4(DNASE1L3):c.730G>A (p.Val244Ile)	DNASE1L3 (V244I +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1518065	NM_004944.4(DNASE1L3):c.729C>G (p.Ile243Met)	DNASE1L3 (I213M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1400382	NM_004944.4(DNASE1L3):c.709G>C (p.Val237Leu)	DNASE1L3 (V207L +1 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 726852	NM_004944.4(DNASE1L3):c.705-3C>T	DNASE1L3	Single nucleotide variant (intron variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GLikely benign
Select item 1485490	NM_004944.4(DNASE1L3):c.671C>T (p.Thr224Met)	DNASE1L3 (T224M +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1355837	NM_004944.4(DNASE1L3):c.601G>A (p.Ala201Thr)	DNASE1L3 (A201T +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1005755	NM_004944.4(DNASE1L3):c.577G>A (p.Gly193Ser)	DNASE1L3 (G163S +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 773866	NM_004944.4(DNASE1L3):c.543G>A (p.Ala181=)	DNASE1L3	Single nucleotide variant (synonymous variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GBenign/Likely benign
Select item 740128	NM_004944.4(DNASE1L3):c.519G>C (p.Thr173=)	DNASE1L3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 732364	NM_004944.4(DNASE1L3):c.501G>A (p.Glu167=)	DNASE1L3	Single nucleotide variant (synonymous variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GBenign/Likely benign
Select item 1404334	NM_004944.4(DNASE1L3):c.448G>A (p.Val150Met)	DNASE1L3 (V120M +1 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 780105	NM_004944.4(DNASE1L3):c.444C>T (p.Asp148=)	DNASE1L3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1424051	NM_004944.4(DNASE1L3):c.437T>C (p.Val146Ala)	DNASE1L3 (V116A +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +2 more	GUncertain significance
Select item 1641723	NM_004944.4(DNASE1L3):c.433+15G>A	DNASE1L3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 1516337	NM_004944.4(DNASE1L3):c.424C>A (p.Pro142Thr)	DNASE1L3 (P142T +1 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1378335	NM_004944.4(DNASE1L3):c.384T>A (p.Asp128Glu)	DNASE1L3 (D128E +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1641478	NM_004944.4(DNASE1L3):c.360T>C (p.His120=)	DNASE1L3	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1464555	NM_004944.4(DNASE1L3):c.359A>G (p.His120Arg)	DNASE1L3 (H90R +1 more)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1672839	NM_004944.4(DNASE1L3):c.320+17C>A	DNASE1L3	Single nucleotide variant (intron variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GLikely benign
Select item 998769	NM_004944.4(DNASE1L3):c.304T>C (p.Tyr102His)	DNASE1L3 (Y102H)	Single nucleotide variant (missense variant +1 more)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1379675	NM_004944.4(DNASE1L3):c.275G>A (p.Arg92Gln)	DNASE1L3 (R92Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 1429970	NM_004944.4(DNASE1L3):c.274C>T (p.Arg92Trp)	DNASE1L3 (R92W)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 720771	NM_004944.4(DNASE1L3):c.231-9G>C	DNASE1L3	Single nucleotide variant (intron variant)	not provided +1 more	GLikely benign
Select item 741274	NM_004944.4(DNASE1L3):c.211C>T (p.Leu71=)	DNASE1L3	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1426007	NM_004944.4(DNASE1L3):c.152G>A (p.Arg51His)	DNASE1L3 (R51H)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1367366	NM_004944.4(DNASE1L3):c.151C>T (p.Arg51Cys)	DNASE1L3 (R51C)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1410671	NM_004944.4(DNASE1L3):c.115A>G (p.Lys39Glu)	DNASE1L3 (K39E)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1442402	NM_004944.4(DNASE1L3):c.112G>C (p.Asp38His)	DNASE1L3 (D38H)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1430966	NM_004944.4(DNASE1L3):c.112G>A (p.Asp38Asn)	DNASE1L3 (D38N)	Single nucleotide variant (missense variant)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance
Select item 1414287	NM_004944.4(DNASE1L3):c.97G>A (p.Glu33Lys)	DNASE1L3 (E33K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1525967	NM_004944.4(DNASE1L3):c.7C>G (p.Arg3Gly)	DNASE1L3 (R3G)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1443268	NM_004944.4(DNASE1L3):c.1A>T (p.Met1Leu)	DNASE1L3 (M1L)	Single nucleotide variant (missense variant +1 more)	Autosomal systemic lupus erythematosus type 16 +1 more	GUncertain significance

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Items: 36