C3805411[trait identifier] AND "Labcorp Genetics (formerly Invitae), L - ClinVar

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2872982	NM_003380.5(VIM):c.82C>G (p.Arg28Gly)	VIM, VIM-AS1 (R28G)	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GUncertain significance
Select item 703473	NM_003380.5(VIM):c.99G>T (p.Thr33=)	VIM-AS1, VIM	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GBenign
Select item 1353044	NM_003380.5(VIM):c.134G>A (p.Arg45His)	VIM, VIM-AS1 (R45H)	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GUncertain significance
Select item 541104	NM_003380.5(VIM):c.167C>A (p.Ser56Tyr)	LOC130003452, VIM +1 more (S56Y)	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GUncertain significance
Select item 779851	NM_003380.5(VIM):c.282C>T (p.Thr94=)	VIM, VIM-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GBenign
Select item 1630176	NM_003380.5(VIM):c.384T>C (p.Asn128=)	VIM, VIM-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GLikely benign
Select item 1630177	NM_003380.5(VIM):c.423A>G (p.Gln141=)	VIM, VIM-AS1	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GLikely benign
Select item 2872983	NM_003380.5(VIM):c.451GAG[2] (p.Glu153del)	VIM, VIM-AS1 (E153del)	Microsatellite (non-coding transcript variant +1 more)	Cataract 30	GUncertain significance
Select item 949490	NM_003380.5(VIM):c.468G>C (p.Glu156Asp)	VIM, VIM-AS1 (E156D)	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30	GUncertain significance
Select item 772763	NM_003380.5(VIM):c.542A>C (p.Asp181Ala)	VIM, VIM-AS1 (D181A)	Single nucleotide variant (non-coding transcript variant +1 more)	Cataract 30 +1 more	GLikely benign
Select item 2893287	NM_003380.5(VIM):c.563+15A>C	LOC130003453, VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 1486484	NM_003380.5(VIM):c.598G>C (p.Glu200Gln)	VIM (E200Q)	Single nucleotide variant (missense variant)	Cataract 30	GUncertain significance
Select item 2091183	NM_003380.5(VIM):c.624+7A>G	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 1110631	NM_003380.5(VIM):c.624+7A>C	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 3006287	NM_003380.5(VIM):c.624+17C>G	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 2012232	NM_003380.5(VIM):c.626A>G (p.Asp209Gly)	VIM (D209G)	Single nucleotide variant (missense variant)	Cataract 30	GUncertain significance
Select item 1316436	NM_003380.5(VIM):c.720+18C>T	VIM	Single nucleotide variant (intron variant)	not provided +1 more	GBenign/Likely benign
Select item 772056	NM_003380.5(VIM):c.749A>G (p.Gln250Arg)	VIM (Q250R)	Single nucleotide variant (missense variant)	Cataract 30	GLikely benign
Select item 959458	NM_003380.5(VIM):c.758A>G (p.His253Arg)	VIM (H253R)	Single nucleotide variant (missense variant)	Cataract 30	GUncertain significance
Select item 1165657	NM_003380.5(VIM):c.807G>T (p.Leu269=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30	GBenign
Select item 474044	NM_003380.5(VIM):c.813C>T (p.Asp271=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30 +1 more	GBenign
Select item 2084511	NM_003380.5(VIM):c.814G>A (p.Val272Ile)	VIM (V272I)	Single nucleotide variant (missense variant)	Cataract 30 +1 more	GUncertain significance
Select item 702034	NM_003380.5(VIM):c.879C>G (p.Ser293=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30 +1 more	GBenign/Likely benign
Select item 2849423	NM_003380.5(VIM):c.882+20G>A	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 1051392	NM_003380.5(VIM):c.911G>A (p.Arg304Gln)	VIM (R304Q)	Single nucleotide variant (missense variant)	Cataract 30	GUncertain significance
Select item 702631	NM_003380.5(VIM):c.987A>G (p.Glu329=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30	GLikely benign
Select item 2080210	NM_003380.5(VIM):c.990G>C (p.Val330=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30	GLikely benign
Select item 1600245	NM_003380.5(VIM):c.1008+18A>G	VIM	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 474043	NM_003380.5(VIM):c.1009-10C>T	VIM	Single nucleotide variant (intron variant)	Cataract 30 +1 more	GBenign
Select item 1127193	NM_003380.5(VIM):c.1009-8C>A	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 2015068	NM_003380.5(VIM):c.1024C>G (p.Arg342Gly)	VIM (R342G)	Single nucleotide variant (missense variant)	Cataract 30	GUncertain significance
Select item 2028925	NM_003380.5(VIM):c.1122G>A (p.Glu374=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30	GLikely benign
Select item 2092384	NM_003380.5(VIM):c.1360-18G>T	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 1654148	NM_003380.5(VIM):c.1360-7dup	VIM	Duplication (intron variant)	Cataract 30	GBenign
Select item 2897515	NM_003380.5(VIM):c.1360-7del	VIM	Deletion (intron variant)	Cataract 30	GBenign
Select item 1577425	NM_003380.5(VIM):c.1360-17T>G	VIM	Single nucleotide variant (intron variant)	Cataract 30	GLikely benign
Select item 2766744	NM_003380.5(VIM):c.1368C>T (p.Asn456=)	VIM	Single nucleotide variant (synonymous variant)	Cataract 30	GLikely benign
Select item 2345133	NM_003380.5(VIM):c.1372A>G (p.Thr458Ala)	VIM (T458A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 962651	NM_003380.5(VIM):c.1374_1375dup (p.Ser459fs)	VIM (S459fs)	Duplication (frameshift variant)	Cataract 30	GUncertain significance

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Items: 39