ClinVar for Gene (Select 79365) - ClinVar

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Links from Gene

Items: 70

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3063250	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835641)x3	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 3057054	NM_030762.3(BHLHE41):c.893C>T (p.Ala298Val)	BHLHE41, SSPN (A298V)	Single nucleotide variant (missense variant)	BHLHE41-related condition	GBenign
Select item 3055569	NM_030762.3(BHLHE41):c.1116G>C (p.Leu372=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	BHLHE41-related condition	GBenign
Select item 3046538	NM_030762.3(BHLHE41):c.844C>T (p.Leu282=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	BHLHE41-related condition	GLikely benign
Select item 3046119	NM_030762.3(BHLHE41):c.1281CGC[5] (p.Ala431_Thr432insAla)	BHLHE41, SSPN	Microsatellite (inframe insertion)	BHLHE41-related condition	GLikely benign
Select item 3045908	NM_030762.3(BHLHE41):c.279G>A (p.Leu93=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	BHLHE41-related condition	GLikely benign
Select item 3041662	NM_030762.3(BHLHE41):c.1323T>A (p.Leu441=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	BHLHE41-related condition	GLikely benign
Select item 3039300	NM_030762.3(BHLHE41):c.1282G>A (p.Ala428Thr)	BHLHE41, SSPN (A428T)	Single nucleotide variant (missense variant)	BHLHE41-related condition	GBenign
Select item 2671607	Single allele	FGD4, FGF23 +278 more	Duplication	not provided	GPathogenic
Select item 2642801	NM_030762.3(BHLHE41):c.100A>C (p.Arg34=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2642800	NM_030762.3(BHLHE41):c.435C>T (p.Tyr145=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2617439	NM_030762.3(BHLHE41):c.860G>A (p.Gly287Asp)	BHLHE41, SSPN (G287D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2615984	NM_030762.3(BHLHE41):c.663C>G (p.Ile221Met)	BHLHE41, SSPN (I221M)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2596509	NM_030762.3(BHLHE41):c.896C>T (p.Ala299Val)	BHLHE41, SSPN (A299V)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2554901	NM_030762.3(BHLHE41):c.34C>G (p.Gln12Glu)	BHLHE41, SSPN (Q12E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2553014	NM_030762.3(BHLHE41):c.658G>A (p.Val220Ile)	BHLHE41, SSPN (V220I)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2546991	NM_030762.3(BHLHE41):c.847G>C (p.Asp283His)	BHLHE41, SSPN (D283H)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2537296	NM_030762.3(BHLHE41):c.1364T>G (p.Leu455Arg)	BHLHE41, SSPN (L455R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2520017	NM_030762.3(BHLHE41):c.820T>A (p.Ser274Thr)	BHLHE41, SSPN (S274T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511990	NM_030762.3(BHLHE41):c.865A>G (p.Ser289Gly)	BHLHE41, SSPN (S289G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2511137	NM_030762.3(BHLHE41):c.1232C>A (p.Ala411Glu)	BHLHE41, SSPN (A411E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2507515	NM_030762.3(BHLHE41):c.901G>A (p.Ala301Thr)	BHLHE41, SSPN (A301T)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2471449	NM_030762.3(BHLHE41):c.1171G>A (p.Gly391Ser)	BHLHE41, SSPN (G391S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2445417	GRCh37/hg19 12p13.33-11.1(chr12:176047-34179852)x4	AKAP3, ETFRF1 +278 more	Copy number gain	Pallister-Killian syndrome	GPathogenic
Select item 2404346	NM_030762.3(BHLHE41):c.950G>A (p.Arg317Lys)	BHLHE41, SSPN (R317K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2401545	NM_030762.3(BHLHE41):c.1381C>G (p.Arg461Gly)	BHLHE41, SSPN (R461G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2379562	NM_030762.3(BHLHE41):c.373C>G (p.Gln125Glu)	BHLHE41, SSPN (Q125E)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2347182	NM_030762.3(BHLHE41):c.1322T>C (p.Leu441Pro)	SSPN, BHLHE41 (L441P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GLikely benign
Select item 2331899	NM_030762.3(BHLHE41):c.767A>G (p.Lys256Arg)	SSPN, BHLHE41 (K256R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2279541	NM_030762.3(BHLHE41):c.883G>C (p.Gly295Arg)	SSPN, BHLHE41 (G295R)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2277249	NM_030762.3(BHLHE41):c.1093C>T (p.Pro365Ser)	BHLHE41, SSPN (P365S)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2261707	NM_030762.3(BHLHE41):c.1016A>C (p.Gln339Pro)	BHLHE41, SSPN (Q339P)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2257146	NM_030762.3(BHLHE41):c.550G>A (p.Val184Ile)	BHLHE41, SSPN (V184I)	Single nucleotide variant (missense variant)	Inborn genetic diseases +1 more	GConflicting classifications of pathogenicity
Select item 2250675	NM_030762.3(BHLHE41):c.188G>A (p.Cys63Tyr)	SSPN, BHLHE41 (C63Y)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2246619	NM_030762.3(BHLHE41):c.932C>A (p.Ala311Asp)	BHLHE41, SSPN (A311D)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2228763	NM_030762.3(BHLHE41):c.467A>G (p.Glu156Gly)	SSPN, BHLHE41 (E156G)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2220678	NM_030762.3(BHLHE41):c.356C>T (p.Ser119Phe)	SSPN, BHLHE41 (S119F)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2218422	NM_030762.3(BHLHE41):c.71A>G (p.Tyr24Cys)	SSPN, BHLHE41 (Y24C)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 2209718	NM_030762.3(BHLHE41):c.349G>A (p.Glu117Lys)	BHLHE41, SSPN (E117K)	Single nucleotide variant (missense variant)	Inborn genetic diseases	GUncertain significance
Select item 1527688	GRCh37/hg19 12p12.3-11.23(chr12:17884992-26704895)	ABCC9, AEBP2 +35 more	Copy number gain	not specified	GPathogenic
Select item 1527672	GRCh37/hg19 12p13.33-q11(chr12:173786-37869301)	C3AR1, CACNA1C +278 more	Copy number gain	not specified	GPathogenic
Select item 1527671	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)	A2M, A2ML1 +278 more	Copy number gain	not specified	GPathogenic
Select item 1340043	GRCh37/hg19 12p12.1-11.22(chr12:23693737-29545102)x1	BCAT1, BHLHE41 +27 more	Copy number loss	not provided	GPathogenic
Select item 815493	GRCh37/hg19 12p13.33-q11(chr12:274676-37869301)x4	ART4, DYRK4 +278 more	Copy number gain	not provided	GPathogenic
Select item 712110	NM_030762.3(BHLHE41):c.1080C>G (p.Ala360=)	BHLHE41, SSPN	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 691289	NM_030762.3(BHLHE41):c.1084T>C (p.Tyr362His)	BHLHE41, SSPN (Y362H)	Single nucleotide variant (missense variant)	Short sleep, familial natural, 1	GAffects
Select item 689124	GRCh37/hg19 12p12.3-11.23(chr12:16141429-27733325)x1	SMCO2, SOX5 +48 more	Copy number loss	not provided	GPathogenic
Select item 686501	GRCh37/hg19 12p13.33-11.1(chr12:173786-34496628)x3	CLEC1B, CLEC2A +278 more	Copy number gain	not provided	GPathogenic
Select item 563991	GRCh37/hg19 12p13.33-q11(chr12:173786-37869107)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563990	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 563989	GRCh37/hg19 12p13.33-11.1(chr12:173786-34835837)x2,3	A2M, A2ML1 +278 more	Copy number gain	not provided	GPathogenic
Select item 443532	GRCh37/hg19 12p13.33-11.22(chr12:173786-28219229)x3	A2M, A2ML1 +256 more	Copy number gain	See cases	GPathogenic
Select item 442150	GRCh37/hg19 12p13.33-11.1(chr12:565369-34835837)x3	A2M, A2ML1 +273 more	Copy number gain	See cases	GLikely pathogenic
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	HMGA2, HNF1A +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 395673	GRCh37/hg19 12p13.33-11.1(chr12:189578-34756150)	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 395235	GRCh37/hg19 12p12.3-11.23(chr12:18037107-26681362)x3	ABCC9, AEBP2 +35 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	AGAP2, ARF3 +1007 more	Copy number gain	See cases	GPathogenic
Select item 253582	GRCh37/hg19 12p13.33-11.1(chr12:148034-34178799)x4	ACSM4, CCND2 +278 more	Copy number gain	See cases	GPathogenic
Select item 253493	GRCh37/hg19 12p13.33-11.1(chr12:89061-34178799)x3	A2M, A2ML1 +278 more	Copy number gain	See cases	GPathogenic
Select item 153962	GRCh38/hg38 12p13.33-11.1(chr12:64620-34682902)x4	A2M, A2M-AS1 +1258 more	Copy number gain	See cases	GPathogenic
Select item 151004	GRCh38/hg38 12p13.33-11.1(chr12:54427-34608071)x4	A2M, A2M-AS1 +1258 more	Copy number gain	See cases	GPathogenic
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	LOC126861648, LOC126861649 +4836 more	Copy number gain	See cases	GPathogenic
Select item 150158	GRCh38/hg38 12p13.33-11.1(chr12:121271-34603261)x3	LOC130007425, LOC130007426 +1257 more	Copy number gain	See cases	GPathogenic
Select item 147419	GRCh38/hg38 12p13.33-11.1(chr12:121255-34603274)x3	A2M, A2M-AS1 +1257 more	Copy number gain	See cases	GPathogenic
Select item 144376	GRCh38/hg38 12p12.1-11.1(chr12:25263833-34064528)x1	ALG10, AMN1 +242 more	Copy number loss	See cases	GPathogenic
Select item 59799	GRCh38/hg38 12p13.33-11.1(chr12:212976-33926913)x4	WBP11, WNK1 +1242 more	Copy number gain	See cases	GPathogenic
Select item 59794	GRCh38/hg38 12p13.33-11.1(chr12:77187-34380176)x3	LOC130007649, LOC130007650 +1258 more	Copy number gain	See cases	GPathogenic
Select item 58988	GRCh38/hg38 12p12.3-11.23(chr12:19295848-27012560)x1	ABCC9, AEBP2 +179 more	Copy number loss	See cases	GPathogenic
Select item 4530	NM_030762.3(BHLHE41):c.1151C>G (p.Pro384Arg)	BHLHE41, SSPN (P384R)	Single nucleotide variant (missense variant)	Short sleep, familial natural, 1	GAffects

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Items: 70