ClinVar for Gene (Select 1783) - ClinVar

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Links from Gene

Items: 60

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3274169	NM_006141.3(DYNC1LI2):c.65C>T (p.Ala22Val)	DYNC1LI2 (A22V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274168	NM_006141.3(DYNC1LI2):c.1223C>T (p.Pro408Leu)	DYNC1LI2 (P369L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274167	NM_006141.3(DYNC1LI2):c.1430G>A (p.Arg477Gln)	DYNC1LI2 (R477Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274166	NM_006141.3(DYNC1LI2):c.38G>A (p.Gly13Asp)	DYNC1LI2 (G13D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274165	NM_006141.3(DYNC1LI2):c.686T>C (p.Val229Ala)	DYNC1LI2 (V190A +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274164	NM_006141.3(DYNC1LI2):c.1133C>T (p.Thr378Met)	DYNC1LI2 (T339M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3255478	NC_000016.9:g.(?_48799549)_(70756330_?)dup	PRMT7, PRSS54 +195 more	Duplication	Chromosome 16q12 duplication syndrome	GLikely pathogenic
Select item 3086464	NM_006141.3(DYNC1LI2):c.838C>T (p.Leu280Phe)	DYNC1LI2 (L203F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086463	NM_006141.3(DYNC1LI2):c.275G>A (p.Ser92Asn)	DYNC1LI2 (S92N)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086462	NM_006141.3(DYNC1LI2):c.274A>G (p.Ser92Gly)	DYNC1LI2 (S92G)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3086461	NM_006141.3(DYNC1LI2):c.25A>C (p.Lys9Gln)	DYNC1LI2 (K9Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086460	NM_006141.3(DYNC1LI2):c.1225G>A (p.Gly409Ser)	DYNC1LI2 (G332S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3086459	NM_006141.3(DYNC1LI2):c.1021G>T (p.Val341Leu)	DYNC1LI2 (V264L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063467	GRCh37/hg19 16q12.2-22.1(chr16:55329260-67180113)x1	ADGRG1, ADGRG3 +85 more	Copy number loss	not specified	GPathogenic
Select item 2684807	GRCh37/hg19 16q21-22.1(chr16:66110708-67240652)x3	B3GNT9, BEAN1 +30 more	Copy number gain	not provided	GUncertain significance
Select item 2646603	NM_006141.3(DYNC1LI2):c.108-6C>T	DYNC1LI2	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 2646602	NM_006141.3(DYNC1LI2):c.222A>G (p.Leu74=)	DYNC1LI2	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2614717	NM_006141.3(DYNC1LI2):c.143G>A (p.Arg48Lys)	DYNC1LI2 (R48K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597633	NM_006141.3(DYNC1LI2):c.307C>T (p.Arg103Cys)	DYNC1LI2 (R103C +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2544787	NM_006141.3(DYNC1LI2):c.77C>T (p.Thr26Ile)	DYNC1LI2 (T26I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2539102	NM_006141.3(DYNC1LI2):c.26A>G (p.Lys9Arg)	DYNC1LI2 (K9R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492674	NM_006141.3(DYNC1LI2):c.877G>A (p.Gly293Ser)	DYNC1LI2 (G216S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2474110	NM_006141.3(DYNC1LI2):c.559C>T (p.Pro187Ser)	DYNC1LI2 (P110S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2458809	NM_006141.3(DYNC1LI2):c.792G>T (p.Gln264His)	DYNC1LI2 (Q264H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2424194	NC_000016.9:g.(?_65821800)_(67208957_?)del	B3GNT9, BEAN1 +25 more	Deletion	not provided	GPathogenic
Select item 2423664	NC_000016.9:g.(?_65821800)_(72146396_?)del	CYB5B, DDX19A +127 more	Deletion	Dyskeratosis congenita, autosomal dominant 6	GUncertain significance
Select item 2351260	NM_006141.3(DYNC1LI2):c.364G>T (p.Ala122Ser)	DYNC1LI2 (A83S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2330629	NM_006141.3(DYNC1LI2):c.314A>G (p.Asn105Ser)	DYNC1LI2 (N66S +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2323921	NM_006141.3(DYNC1LI2):c.406G>A (p.Val136Ile)	DYNC1LI2 (V136I +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2240875	NM_006141.3(DYNC1LI2):c.792G>C (p.Gln264His)	DYNC1LI2 (Q264H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2221088	NM_006141.3(DYNC1LI2):c.1051G>A (p.Asp351Asn)	DYNC1LI2 (D312N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 1676307	GRCh37/hg19 16q11.2-24.3(chr16:46503968-90155062)x3	AARS1, ABCC11 +368 more	Copy number gain	not provided	GPathogenic
Select item 973025	GRCh37/hg19 16q21-24.3(chr16:61524229-90155062)x3	AARS1, ACD +268 more	Copy number gain	not provided	Gnot provided
Select item 815823	GRCh37/hg19 16q21-22.1(chr16:65669673-70180183)x1	EXOC3L1, ESRP2 +95 more	Copy number loss	not provided	GPathogenic
Select item 808176	GRCh37/hg19 16q21-22.1(chr16:64981506-66806661)x3	CKLF-CMTM1, CMTM4 +10 more	Copy number gain	not provided	GUncertain significance
Select item 564331	GRCh37/hg19 16q12.2-22.2(chr16:54416050-72453266)x3	AARS1, ACD +194 more	Copy number gain	not provided	GPathogenic
Select item 523162	GRCh37/hg19 16q11.2-24.3(chr16:46455960-90354753)x1	CA7, COG8 +368 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 523156	GRCh37/hg19 16q11.2-24.3(chr16:46497599-90354753)x1	KCTD19, KIAA0513 +368 more	Copy number loss	Poly (ADP-Ribose) polymerase inhibitor response	Gdrug response
Select item 443126	GRCh37/hg19 16p13.2-q24.3(chr16:9273328-89548493)x3	CBLN1, CCDC102A +591 more	Copy number gain	See cases	GUncertain significance
Select item 443121	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)x3	AARS1, ABAT +811 more	Copy number gain	See cases	GPathogenic
Select item 443120	GRCh37/hg19 16p13.3-q24.3(chr16:85881-90155062)	CCL22, CCNF +811 more	Copy number gain	See cases	GPathogenic
Select item 442784	GRCh37/hg19 16q21-22.1(chr16:66537021-67369281)x3	B3GNT9, CA7 +35 more	Copy number gain	See cases	GUncertain significance
Select item 442214	GRCh37/hg19 16q13-24.3(chr16:57051473-89797669)x3	AARS1, ACD +292 more	Copy number gain	See cases	GPathogenic
Select item 395502	GRCh37/hg19 16p13.3-q24.3(chr16:69193-90274381)x3	ABCC6, BCL7C +811 more	Copy number gain	See cases	GPathogenic
Select item 221523	GRCh37/hg19 16q12.2-22.2(chr16:55359026-70884455)x1	AARS1, ACD +174 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221392	GRCh37/hg19 16q11.2-24.3(chr16:46615804-90142285)x1	ATXN1L, B3GNT9 +368 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221345	Single allele	ADGRG5, CFAP263 +324 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 155685	GRCh38/hg38 16q12.1-22.1(chr16:49685521-68401712)x3	LOC130059125, LOC130059126 +675 more	Copy number gain	See cases	GPathogenic
Select item 155675	GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3	LOC130059420, LOC130059421 +869 more	Copy number gain	See cases	GPathogenic
Select item 155358	GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	MIR138-2, MIR140 +1738 more	Copy number gain	See cases	GPathogenic
Select item 154511	GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	LOC130059829, LOC130059830 +1429 more	Copy number gain	See cases	GPathogenic
Select item 150599	GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	LOC130059834, LOC130059835 +1424 more	Copy number gain	See cases	GPathogenic
Select item 146601	GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3	AARS1, ACD +939 more	Copy number gain	See cases	GPathogenic
Select item 145310	GRCh38/hg38 16q21-22.1(chr16:66245888-67473023)x1	ATP6V0D1, B3GNT9 +113 more	Copy number loss	See cases	GPathogenic
Select item 59494	GRCh38/hg38 16q22.1(chr16:66694180-67865445)x1	ACD, AGRP +155 more	Copy number loss	See cases	GPathogenic
Select item 59493	GRCh38/hg38 16q21-22.1(chr16:64311275-68062011)x1	ACD, AGRP +217 more	Copy number loss	See cases	GPathogenic
Select item 59491	GRCh38/hg38 16q21-22.1(chr16:62179331-67770414)x1	ACD, AGRP +176 more	Copy number loss	See cases	GPathogenic
Select item 58645	GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	LOC108281164, LOC109029536 +1426 more	Copy number gain	See cases	GPathogenic
Select item 58632	GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	LOC130059197, LOC130059198 +575 more	Copy number gain	See cases	GPathogenic
Select item 58630	GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3	LOC130059330, LOC130059331 +599 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 60