"Athena Diagnostics"[submitter] AND "NDRG1"[gene] - ClinVar

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Items: 25

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 655683	NM_006096.4(NDRG1):c.1153G>A (p.Ala385Thr)	NDRG1 (A385T +3 more)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 447748	NM_006096.4(NDRG1):c.1101C>T (p.Ser367=)	NDRG1	Single nucleotide variant (synonymous variant)	not specified +4 more	GConflicting classifications of pathogenicity
Select item 476844	NM_006096.4(NDRG1):c.1088G>A (p.Arg363His)	NDRG1 (R363H +3 more)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 543351	NM_006096.4(NDRG1):c.1085G>A (p.Ser362Asn)	NDRG1 (S362N +3 more)	Single nucleotide variant (missense variant)	Charcot-Marie-Tooth disease type 4 +1 more	GUncertain significance
Select item 639524	NM_006096.4(NDRG1):c.1053_1082del (p.340TRSRSHTSEG[2])	NDRG1	Deletion (inframe_deletion)	Inborn genetic diseases +4 more	GConflicting classifications of pathogenicity
Select item 447747	NM_006096.4(NDRG1):c.1070G>C (p.Ser357Thr)	NDRG1 (S357T +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 937984	NM_006096.4(NDRG1):c.1057C>T (p.Arg353Cys)	NDRG1 (R272C +3 more)	Single nucleotide variant (missense variant)	not provided +2 more	GUncertain significance
Select item 447750	NM_006096.4(NDRG1):c.965G>A (p.Arg322His)	NDRG1 (R322H +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 362033	NM_006096.4(NDRG1):c.892-5C>T	NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign
Select item 2684272	NM_006096.4(NDRG1):c.891+3G>C	NDRG1	Single nucleotide variant (intron variant)	not provided	GUncertain significance
Select item 1806902	NM_006096.4(NDRG1):c.816C>G (p.Cys272Trp)	NDRG1 (C191W +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 379907	NM_006096.4(NDRG1):c.789G>A (p.Ser263=)	LOC126860531, NDRG1	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease type 4 +5 more	GConflicting classifications of pathogenicity
Select item 1806904	NM_006096.4(NDRG1):c.773T>C (p.Val258Ala)	LOC126860531, NDRG1 (V177A +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 138434	NM_006096.4(NDRG1):c.756-5C>T	LOC126860531, NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign
Select item 138433	NM_006096.4(NDRG1):c.755+10T>C	LOC126860531, NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign
Select item 447749	NM_006096.4(NDRG1):c.595-6A>G	NDRG1	Single nucleotide variant (intron variant)	Charcot-Marie-Tooth disease type 4 +1 more	GUncertain significance
Select item 695697	NM_006096.4(NDRG1):c.528C>T (p.Ala176=)	NDRG1	Single nucleotide variant (synonymous variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 219798	NM_006096.4(NDRG1):c.507G>A (p.Ala169=)	NDRG1	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign
Select item 362039	NM_006096.4(NDRG1):c.306C>T (p.Gly102=)	NDRG1	Single nucleotide variant (synonymous variant)	Charcot-Marie-Tooth disease type 4 +3 more	GBenign/Likely benign
Select item 362040	NM_006096.4(NDRG1):c.199A>G (p.Met67Val)	NDRG1 (M67V +1 more)	Single nucleotide variant (missense variant +2 more)	Charcot-Marie-Tooth disease type 4 +4 more	GBenign/Likely benign
Select item 245649	NM_006096.4(NDRG1):c.122A>G (p.His41Arg)	NDRG1 (H41R)	Single nucleotide variant (missense variant +2 more)	Charcot-Marie-Tooth disease type 4 +5 more	GUncertain significance
Select item 2684271	NM_006096.4(NDRG1):c.77T>C (p.Leu26Pro)	NDRG1 (L26P)	Single nucleotide variant (missense variant +2 more)	not provided	GUncertain significance
Select item 259916	NM_006096.4(NDRG1):c.64-6T>C	NDRG1	Single nucleotide variant (intron variant)	not provided +4 more	GBenign
Select item 220934	NM_006096.4(NDRG1):c.31G>A (p.Ala11Thr)	NDRG1 (A11T)	Single nucleotide variant (missense variant +2 more)	NDRG1-related disorder +5 more	GConflicting classifications of pathogenicity
Select item 1806903	NM_006096.4(NDRG1):c.-18-8C>G	NDRG1	Single nucleotide variant (intron variant)	not provided	GUncertain significance

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Items: 25