C1853371[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1809694	NM_002500.5(NEUROD1):c.*1A>G	NEUROD1	Single nucleotide variant (3 prime UTR variant)	Maturity-onset diabetes of the young type 6 +1 more	GLikely benign
Select item 1307264	NM_002500.5(NEUROD1):c.1055C>T (p.Ala352Val)	NEUROD1 (A352V)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 896246	NM_002500.5(NEUROD1):c.1055C>A (p.Ala352Asp)	NEUROD1 (A352D)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1584195	NM_002500.5(NEUROD1):c.1050C>G (p.Leu350=)	NEUROD1	Single nucleotide variant (synonymous variant)	Maturity-onset diabetes of the young type 6 +2 more	GLikely benign
Select item 1001142	NM_002500.5(NEUROD1):c.1031G>A (p.Arg344Gln)	NEUROD1 (R344Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 950336	NM_002500.5(NEUROD1):c.1013G>C (p.Ser338Thr)	NEUROD1 (S338T)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1053839	NM_002500.5(NEUROD1):c.917C>T (p.Ala306Val)	NEUROD1 (A306V)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1026908	NM_002500.5(NEUROD1):c.794C>G (p.Thr265Ser)	NEUROD1 (T265S)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1417052	NM_002500.5(NEUROD1):c.761A>C (p.Glu254Ala)	NEUROD1 (E254A)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1038985	NM_002500.5(NEUROD1):c.758T>C (p.Leu253Pro)	NEUROD1 (L253P)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1462185	NM_002500.5(NEUROD1):c.746A>G (p.Tyr249Cys)	NEUROD1 (Y249C)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 972116	NM_002500.5(NEUROD1):c.741C>A (p.His247Gln)	NEUROD1 (H247Q)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 333038	NM_002500.5(NEUROD1):c.646G>A (p.Val216Ile)	NEUROD1 (V216I)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1367987	NM_002500.5(NEUROD1):c.616C>G (p.His206Asp)	NEUROD1 (H206D)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1001015	NM_002500.5(NEUROD1):c.616C>A (p.His206Asn)	NEUROD1 (H206N)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 897855	NM_002500.5(NEUROD1):c.418A>G (p.Ile140Val)	NEUROD1 (I140V)	Single nucleotide variant (missense variant)	Type 2 diabetes mellitus +2 more	GUncertain significance
Select item 1014823	NM_002500.5(NEUROD1):c.284G>A (p.Arg95His)	NEUROD1 (R95H)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 836918	NM_002500.5(NEUROD1):c.260A>G (p.Lys87Arg)	NEUROD1 (K87R)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 1019474	NM_002500.5(NEUROD1):c.222GGA[1] (p.Glu75del)	NEUROD1 (E75del)	Microsatellite (inframe_deletion)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1085896	NM_002500.5(NEUROD1):c.195C>T (p.Asp65=)	NEUROD1	Single nucleotide variant (synonymous variant)	not provided +2 more	GLikely benign
Select item 1659484	NM_002500.5(NEUROD1):c.189T>C (p.Asp63=)	NEUROD1	Single nucleotide variant (synonymous variant)	Maturity-onset diabetes of the young type 6 +2 more	GLikely benign
Select item 1503008	NM_002500.5(NEUROD1):c.175G>C (p.Glu59Gln)	NEUROD1 (E59Q)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 333039	NM_002500.5(NEUROD1):c.129C>A (p.Leu43=)	NEUROD1	Single nucleotide variant (synonymous variant)	Maturity-onset diabetes of the young type 6 +3 more	GBenign/Likely benign
Select item 1369525	NM_002500.5(NEUROD1):c.112A>G (p.Lys38Glu)	NEUROD1 (K38E)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1493150	NM_002500.5(NEUROD1):c.94G>A (p.Glu32Lys)	NEUROD1 (E32K)	Single nucleotide variant (missense variant)	Maturity-onset diabetes of the young type 6 +2 more	GUncertain significance
Select item 1438002	NM_002500.5(NEUROD1):c.79C>T (p.Leu27Phe)	NEUROD1 (L27F)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 899006	NM_002500.5(NEUROD1):c.37G>A (p.Glu13Lys)	NEUROD1 (E13K)	Single nucleotide variant (missense variant)	Type 2 diabetes mellitus +1 more	GUncertain significance

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Items: 27