"Ambry Genetics"[submitter] AND "LRRC55"[gene] - ClinVar

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2608498	NM_001005210.2(LRRC55):c.13C>T (p.Pro5Ser)	LRRC55 (P5S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2204418	NM_001005210.4(LRRC55):c.-60G>A	LRRC55	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2291695	NM_001005210.4(LRRC55):c.-36G>A	LRRC55	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2472328	NM_001005210.4(LRRC55):c.54G>A (p.Met18Ile)	LRRC55 (M18I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2559255	NM_001005210.4(LRRC55):c.67C>T (p.Leu23Phe)	LRRC55 (L23F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120808	NM_001005210.4(LRRC55):c.118G>A (p.Val40Ile)	LRRC55 (V40I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2212312	NM_001005210.4(LRRC55):c.133C>T (p.Arg45Cys)	LRRC55 (R45C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291694	NM_001005210.4(LRRC55):c.143T>G (p.Val48Gly)	LRRC55 (V48G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291690	NM_001005210.4(LRRC55):c.164G>A (p.Arg55Gln)	LRRC55 (R55Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2256578	NM_001005210.4(LRRC55):c.171C>G (p.Phe57Leu)	LRRC55 (F57L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291692	NM_001005210.4(LRRC55):c.175G>A (p.Val59Met)	LRRC55 (V59M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455477	NM_001005210.4(LRRC55):c.227G>A (p.Arg76His)	LRRC55 (R76H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291691	NM_001005210.4(LRRC55):c.265A>G (p.Met89Val)	LRRC55 (M89V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2216382	NM_001005210.4(LRRC55):c.278T>G (p.Val93Gly)	LRRC55 (V93G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2239731	NM_001005210.4(LRRC55):c.316C>T (p.Arg106Trp)	LRRC55 (R106W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2248856	NM_001005210.4(LRRC55):c.351C>G (p.His117Gln)	LOC124489741, LRRC55 (H117Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3291693	NM_001005210.4(LRRC55):c.443C>T (p.Pro148Leu)	LOC124489741, LRRC55 (P148L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2336070	NM_001005210.4(LRRC55):c.455G>C (p.Arg152Thr)	LOC124489741, LRRC55 (R152T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2457070	NM_001005210.4(LRRC55):c.685G>A (p.Gly229Ser)	LRRC55 (G229S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2359080	NM_001005210.4(LRRC55):c.700G>A (p.Glu234Lys)	LRRC55 (E234K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120809	NM_001005210.4(LRRC55):c.742G>T (p.Ala248Ser)	LRRC55 (A248S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2598426	NM_001005210.4(LRRC55):c.787T>A (p.Phe263Ile)	LRRC55 (F263I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3120810	NM_001005210.4(LRRC55):c.799G>A (p.Val267Met)	LRRC55 (V267M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463183	NM_001005210.4(LRRC55):c.889G>A (p.Glu297Lys)	LRRC55 (E297K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar

Result Filters

Classification type

Germline classification

Types of conflicts

Molecular consequence

Variation type

Variation size

Variant length

Review status

Additional filters

Search results

Items: 24