LILRA4[gene] - ClinVar

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

Search results

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 151454	GRCh37/hg19 19q13.42(chr19:54769799-54864136)x3	LOC126862931, LAIR1 +10 more	Copy number gain	See cases	GLikely benign
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 more	Copy number gain	See cases	GPathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065034, LOC130065035 +761 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 153721	GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	A1BG, A1BG-AS1 +547 more	Copy number gain	See cases	GPathogenic
Select item 144762	GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	SSC5D, SYT5 +553 more	Copy number gain	See cases	GPathogenic
Select item 144709	GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	TMC4, TMEM150B +537 more	Copy number gain	See cases	GPathogenic
Select item 2535554	NM_012276.5(LILRA4):c.1489G>A (p.Glu497Lys)	LILRA4 (E497K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2348903	NM_012276.5(LILRA4):c.1483C>G (p.Pro495Ala)	LILRA4 (P495A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2264618	NM_012276.5(LILRA4):c.1471A>G (p.Arg491Gly)	LILRA4 (R491G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2393322	NM_012276.5(LILRA4):c.1423C>G (p.Pro475Ala)	LILRA4 (P475A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2509957	NM_012276.5(LILRA4):c.1348A>G (p.Met450Val)	LILRA4 (M450V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374623	NM_012276.5(LILRA4):c.1346G>A (p.Arg449His)	LILRA4 (R449H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558297	NM_012276.5(LILRA4):c.1307C>T (p.Ala436Val)	LILRA4 (A436V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2308451	NM_012276.5(LILRA4):c.1249G>A (p.Val417Ile)	LILRA4 (V417I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2387930	NM_012276.5(LILRA4):c.1219T>A (p.Ser407Thr)	LILRA4 (S407T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2545361	NM_012276.5(LILRA4):c.1206C>A (p.Asn402Lys)	LILRA4 (N402K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118755	NM_012276.5(LILRA4):c.1204A>G (p.Asn402Asp)	LILRA4 (N402D)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3118754	NM_012276.5(LILRA4):c.1114G>A (p.Gly372Arg)	LILRA4 (G372R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3118753	NM_012276.5(LILRA4):c.1104A>C (p.Arg368Ser)	LILRA4 (R368S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412294	NM_012276.5(LILRA4):c.998C>T (p.Thr333Met)	LILRA4 (T333M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118766	NM_012276.5(LILRA4):c.958A>G (p.Ile320Val)	LILRA4 (I320V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118765	NM_012276.5(LILRA4):c.953G>A (p.Gly318Glu)	LILRA4 (G318E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118763	NM_012276.5(LILRA4):c.893C>T (p.Ala298Val)	LILRA4 (A298V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510463	NM_012276.5(LILRA4):c.889G>A (p.Gly297Ser)	LILRA4 (G297S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118762	NM_012276.5(LILRA4):c.865T>C (p.Tyr289His)	LILRA4 (Y289H)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2471746	NM_012276.5(LILRA4):c.860G>C (p.Arg287Pro)	LILRA4 (R287P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290687	NM_012276.5(LILRA4):c.847A>T (p.Ser283Cys)	LILRA4 (S283C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310116	NM_012276.5(LILRA4):c.847A>G (p.Ser283Gly)	LILRA4 (S283G)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3290685	NM_012276.5(LILRA4):c.806G>A (p.Arg269Gln)	LILRA4 (R269Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2548440	NM_012276.5(LILRA4):c.758A>G (p.Tyr253Cys)	LILRA4 (Y253C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2460180	NM_012276.5(LILRA4):c.709G>A (p.Gly237Arg)	LILRA4 (G237R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2251581	NM_012276.5(LILRA4):c.704C>T (p.Thr235Ile)	LILRA4 (T235I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118761	NM_012276.5(LILRA4):c.669G>C (p.Lys223Asn)	LILRA4 (K223N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290688	NM_012276.5(LILRA4):c.658G>T (p.Val220Leu)	LILRA4 (V220L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118760	NM_012276.5(LILRA4):c.633C>A (p.Asp211Glu)	LILRA4 (D211E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118759	NM_012276.5(LILRA4):c.449G>C (p.Gly150Ala)	LILRA4 (G150A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305039	NM_012276.5(LILRA4):c.445C>G (p.Leu149Val)	LILRA4 (L149V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2508989	NM_012276.5(LILRA4):c.436C>T (p.Arg146Trp)	LILRA4 (R146W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118758	NM_012276.5(LILRA4):c.415G>A (p.Val139Met)	LILRA4 (V139M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118757	NM_012276.5(LILRA4):c.146G>A (p.Cys49Tyr)	LILRA4 (C49Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3290686	NM_012276.5(LILRA4):c.129C>A (p.Asn43Lys)	LILRA4 (N43K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3118756	NM_012276.5(LILRA4):c.126T>A (p.His42Gln)	LILRA4 (H42Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2531850	NM_012276.5(LILRA4):c.106G>A (p.Gly36Ser)	LILRA4 (G36S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3118764	NM_012276.5(LILRA4):c.92T>C (p.Leu31Pro)	LILRA4 (L31P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2650449	NM_012276.5(LILRA4):c.33T>C (p.Phe11=)	LILRA4	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2533812	NM_012276.5(LILRA4):c.28T>C (p.Phe10Leu)	LILRA4 (F10L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2383316	NM_012276.5(LILRA4):c.26T>C (p.Leu9Pro)	LILRA4 (L9P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351536	NM_012276.5(LILRA4):c.17C>A (p.Thr6Lys)	LILRA4 (T6K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2672793	GRCh37/hg19 19q13.42(chr19:54544215-54881884)x3	CNOT3, LAIR1 +18 more	Copy number gain	not provided	GUncertain significance
Select item 1443808	NC_000019.9:g.(?_54297303)_(55678016_?)dup	CACNG6, CACNG7 +51 more	Duplication	not provided	GUncertain significance
Select item 980772	GRCh37/hg19 19q13.42-13.43(chr19:54334195-56434037)x3	TMC4, TMEM150B +87 more	Copy number gain	not provided	GUncertain significance
Select item 980771	GRCh37/hg19 19q13.42(chr19:54659105-54916280)x3	CNOT3, LAIR1 +12 more	Copy number gain	not provided	GUncertain significance
Select item 980768	GRCh37/hg19 19q13.33-13.43(chr19:48463931-57095254)x3	PPP1R15A, PPP2R1A +308 more	Copy number gain	not provided	GPathogenic
Select item 816093	GRCh37/hg19 19q13.42(chr19:54701333-55536206)x3	CDC42EP5, FCAR +28 more	Copy number gain	not provided	GUncertain significance
Select item 816092	GRCh37/hg19 19q13.42(chr19:54474844-55181741)x3	CACNG6, CACNG8 +29 more	Copy number gain	not provided	GUncertain significance
Select item 564606	GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	ZNF548, ZNF549 +157 more	Copy number gain	not provided	GPathogenic
Select item 564602	GRCh37/hg19 19q13.42(chr19:53867570-55833460)x3	BRSK1, CACNG6 +68 more	Copy number gain	not provided	GUncertain significance
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	PGLYRP1, PGLYRP2 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	TMC4, TMED1 +1364 more	Copy number gain	See cases	GPathogenic
Select item 425531	GRCh37/hg19 19q13.42(chr19:54754462-54866330)x3	LAIR1, LILRA3 +4 more	Copy number gain	not provided	GUncertain significance
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 221404	GRCh37/hg19 19q13.42(chr19:54710237-55648526)x1	LILRB3, CDC42EP5 +32 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221353	chr19:54754752-55624113 complex variant	FCAR, EPS8L1 +28 more	Complex	Breast ductal adenocarcinoma	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: 68