ClinVar for Gene (Select 83417) - ClinVar

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Links from Gene

Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3278400	NM_031282.3(FCRL4):c.802G>A (p.Gly268Ser)	FCRL4, LOC126805881 (G268S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278399	NM_031282.3(FCRL4):c.1009C>G (p.Gln337Glu)	FCRL4 (Q337E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278398	NM_031282.3(FCRL4):c.1544G>A (p.Ser515Asn)	FCRL4 (S515N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278397	NM_031282.3(FCRL4):c.1255G>T (p.Gly419Cys)	FCRL4 (G419C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3278396	NM_031282.3(FCRL4):c.1096G>A (p.Gly366Ser)	FCRL4 (G366S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3242278	GRCh37/hg19 1q22-23.2(chr1:155709113-159191078)x3	ACKR1, AIM2 +80 more	Copy number gain	not provided	GLikely pathogenic
Select item 3094218	NM_031282.3(FCRL4):c.991A>G (p.Ser331Gly)	FCRL4 (S331G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094217	NM_031282.3(FCRL4):c.899C>T (p.Ala300Val)	FCRL4 (A300V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3094215	NM_031282.3(FCRL4):c.730C>G (p.Pro244Ala)	FCRL4, LOC126805881 (P244A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094214	NM_031282.3(FCRL4):c.649C>T (p.Pro217Ser)	FCRL4, LOC126805881 (P217S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094213	NM_031282.3(FCRL4):c.427C>A (p.Leu143Ile)	FCRL4, LOC126805881 (L143I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3094212	NM_031282.3(FCRL4):c.1301G>T (p.Gly434Val)	FCRL4 (G434V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094211	NM_031282.3(FCRL4):c.1269C>G (p.Asp423Glu)	FCRL4 (D423E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094210	NM_031282.3(FCRL4):c.1259T>C (p.Phe420Ser)	FCRL4 (F420S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3094209	NM_031282.3(FCRL4):c.1063G>C (p.Gly355Arg)	FCRL4 (G355R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062988	GRCh37/hg19 1q21.1-23.1(chr1:144368497-158992086)x3	ACP6, ADAM15 +315 more	Copy number gain	not specified	GPathogenic
Select item 2621274	NM_031282.3(FCRL4):c.1123G>A (p.Val375Ile)	FCRL4 (V375I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2580317	GRCh37/hg19 1q12-23.1(chr1:142535935-157648813)x3	ACP6, ADAM15 +293 more	Copy number gain	Chromosome 1q21.1 duplication syndrome	GPathogenic
Select item 2551104	NM_031282.3(FCRL4):c.1046T>A (p.Ile349Asn)	FCRL4 (I349N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550371	NM_031282.3(FCRL4):c.1391C>G (p.Ser464Cys)	FCRL4 (S464C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535040	NM_031282.3(FCRL4):c.940G>A (p.Glu314Lys)	FCRL4 (E314K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533629	NM_031282.3(FCRL4):c.1493C>T (p.Thr498Ile)	FCRL4 (T498I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495172	NM_031282.3(FCRL4):c.357G>C (p.Leu119Phe)	FCRL4, LOC126805881 (L119F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486600	NM_031282.3(FCRL4):c.1012C>T (p.Arg338Cys)	FCRL4 (R338C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2484379	NM_031282.3(FCRL4):c.526G>A (p.Val176Ile)	FCRL4, LOC126805881 (V176I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2455642	NM_031282.3(FCRL4):c.823C>A (p.Pro275Thr)	FCRL4, LOC126805881 (P275T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411296	NM_031282.3(FCRL4):c.644A>G (p.Gln215Arg)	FCRL4, LOC126805881 (Q215R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410641	NM_031282.3(FCRL4):c.612G>T (p.Glu204Asp)	FCRL4, LOC126805881 (E204D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2386927	NM_031282.3(FCRL4):c.533G>A (p.Arg178Lys)	FCRL4, LOC126805881 (R178K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2375072	NM_031282.3(FCRL4):c.1084G>A (p.Asp362Asn)	FCRL4 (D362N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374528	NM_031282.3(FCRL4):c.262C>T (p.Arg88Trp)	FCRL4 (R88W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2245674	NM_031282.3(FCRL4):c.1268A>G (p.Asp423Gly)	FCRL4 (D423G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1252028	NM_031282.3(FCRL4):c.847+1G>A	FCRL4, LOC126805881	Single nucleotide variant (splice donor variant)	not specified	GUncertain significance
Select item 1003645	NC_000001.10:g.(?_130980840)_(248900000_?)dup	FCGR3A, LCE3C +956 more	Duplication	Parathyroid carcinoma +2 more	GUncertain significance
Select item 783951	NM_031282.3(FCRL4):c.764A>G (p.Asn255Ser)	FCRL4, LOC126805881 (N255S)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 783950	NM_031282.3(FCRL4):c.1370A>G (p.Lys457Arg)	FCRL4 (K457R)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 775612	NM_031282.3(FCRL4):c.1221G>C (p.Leu407=)	FCRL4	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 688082	GRCh37/hg19 1q23.1-24.2(chr1:157321299-167391423)x1	ACKR1, ADAMTS4 +132 more	Copy number loss	not provided	GPathogenic
Select item 565186	GRCh37/hg19 1q23.1(chr1:157347489-157804172)x3	FCRL1, FCRL5 +4 more	Copy number gain	not provided	GUncertain significance
Select item 565183	GRCh37/hg19 1q22-23.1(chr1:155636337-158024499)x1	ARHGEF11, ARHGEF2 +57 more	Copy number loss	not provided	GPathogenic
Select item 442387	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)	CD34, CD46 +2014 more	Copy number gain	See cases	GPathogenic
Select item 442386	GRCh37/hg19 1p36.33-q44(chr1:849467-249224684)x3	GPATCH2, GPATCH3 +2014 more	Copy number gain	See cases	GPathogenic
Select item 155448	GRCh38/hg38 1q21.2-25.2(chr1:149854269-180267197)x3	LOC129931453, LOC129931454 +1585 more	Copy number gain	See cases	GPathogenic
Select item 151159	GRCh38/hg38 1q21.3-23.1(chr1:154566501-157624084)x3	ADAM15, ADAM15-EFNA4 +297 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 44