"LZTFL1-related condition"[Disease/phenotype] AND "PreventionGenetics, - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 943991	NM_020347.4(LZTFL1):c.798G>C (p.Gln266His)	LZTFL1 (Q266H +1 more)	Single nucleotide variant (missense variant +2 more)	LZTFL1-related condition +2 more	GUncertain significance
Select item 1356804	NM_020347.4(LZTFL1):c.766A>G (p.Met256Val)	LZTFL1 (M256V +2 more)	Single nucleotide variant (missense variant +1 more)	LZTFL1-related condition +2 more	GUncertain significance
Select item 1148644	NM_020347.4(LZTFL1):c.735C>T (p.His245=)	LZTFL1	Single nucleotide variant (synonymous variant +1 more)	LZTFL1-related condition +1 more	GLikely benign
Select item 963919	NM_020347.4(LZTFL1):c.724A>G (p.Thr242Ala)	LZTFL1 (T242A +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 733625	NM_020347.4(LZTFL1):c.685A>G (p.Lys229Glu)	LZTFL1 (K229E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GBenign/Likely benign
Select item 1169361	NM_020347.4(LZTFL1):c.646G>A (p.Ala216Thr)	LZTFL1 (A199T +2 more)	Single nucleotide variant (missense variant +1 more)	LZTFL1-related condition +2 more	GBenign/Likely benign
Select item 1022800	NM_020347.4(LZTFL1):c.454A>G (p.Lys152Glu)	LZTFL1 (K135E +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 741647	NM_020347.4(LZTFL1):c.420A>G (p.Pro140=)	LZTFL1	Single nucleotide variant (synonymous variant +1 more)	LZTFL1-related condition +1 more	GLikely benign
Select item 3042267	NM_020347.4(LZTFL1):c.363G>A (p.Glu121=)	LZTFL1	Single nucleotide variant (synonymous variant +1 more)	LZTFL1-related condition	GLikely benign
Select item 1014254	NM_020347.4(LZTFL1):c.361G>A (p.Glu121Lys)	LZTFL1 (E104K +2 more)	Single nucleotide variant (missense variant +1 more)	not provided +3 more	GUncertain significance
Select item 3061524	NM_020347.4(LZTFL1):c.340G>A (p.Val114Ile)	LZTFL1 (V110I +3 more)	Single nucleotide variant (missense variant +1 more)	LZTFL1-related condition	GUncertain significance
Select item 1964607	NM_020347.4(LZTFL1):c.303C>T (p.Asp101=)	LZTFL1	Single nucleotide variant (synonymous variant +1 more)	not provided +1 more	GLikely benign
Select item 3029918	NM_020347.4(LZTFL1):c.231C>G (p.Ala77=)	LZTFL1	Single nucleotide variant (synonymous variant +1 more)	LZTFL1-related condition	GLikely benign
Select item 1373766	NM_020347.4(LZTFL1):c.155A>T (p.Asp52Val)	LZTFL1 (D35V +2 more)	Single nucleotide variant (missense variant +1 more)	LZTFL1-related condition +1 more	GUncertain significance
Select item 1019150	NM_020347.4(LZTFL1):c.56G>A (p.Arg19His)	LZTFL1 (R19H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +2 more	GUncertain significance
Select item 3005975	NM_020347.4(LZTFL1):c.42T>C (p.Val14=)	LZTFL1	Single nucleotide variant (5 prime UTR variant +2 more)	not provided +1 more	GLikely benign
Select item 3029602	NM_001276379.2(LZTFL1):c.66C>T (p.His22=)	LZTFL1	Single nucleotide variant (5 prime UTR variant +3 more)	LZTFL1-related condition	GLikely benign
Select item 3039964	NM_001276379.2(LZTFL1):c.52T>G (p.Leu18Val)	LZTFL1 (L18V)	Single nucleotide variant (5 prime UTR variant +3 more)	LZTFL1-related condition	GUncertain significance
Select item 3059402	NM_001276379.2(LZTFL1):c.36G>A (p.Gln12=)	LZTFL1	Single nucleotide variant (5 prime UTR variant +3 more)	LZTFL1-related condition	GLikely benign
Select item 2634303	NM_001276379.2(LZTFL1):c.28-5T>G	LZTFL1	Single nucleotide variant (intron variant)	LZTFL1-related condition	GUncertain significance
Select item 3037258	NM_001276379.2(LZTFL1):c.26T>C (p.Met9Thr)	LZTFL1 (M9T)	Single nucleotide variant (5 prime UTR variant +2 more)	LZTFL1-related condition	GLikely benign
Select item 3049487	NM_001276379.2(LZTFL1):c.10C>G (p.Gln4Glu)	LZTFL1 (Q4E)	Single nucleotide variant (5 prime UTR variant +2 more)	LZTFL1-related condition	GUncertain significance
Select item 3051858	NM_001276378.2(LZTFL1):c.-170T>G	LZTFL1	Single nucleotide variant (5 prime UTR variant +1 more)	LZTFL1-related condition	GLikely benign

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Items: 23