ClinVar for Gene (Select 100529251) - ClinVar

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Links from Gene

Items: 56

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3267992	NM_052999.4(CMTM1):c.325G>A (p.Ala109Thr)	CKLF-CMTM1, CMTM1 (A109T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267991	NM_052999.4(CMTM1):c.281C>T (p.Pro94Leu)	CKLF-CMTM1, CMTM1 (P94L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267485	NM_001204099.2(CKLF-CMTM1):c.166A>G (p.Ile56Val)	CKLF, CKLF-CMTM1 (I56V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267484	NM_016951.4(CKLF):c.371A>G (p.Asp124Gly)	CKLF, CKLF-CMTM1 (D92G +3 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 3146256	NM_052999.4(CMTM1):c.94A>G (p.Ser32Gly)	CKLF-CMTM1, CMTM1 (S32G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3145251	NM_001204099.2(CKLF-CMTM1):c.13C>A (p.Gln5Lys)	CKLF, CKLF-CMTM1 (Q5K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3145250	NM_016951.4(CKLF):c.372C>G (p.Asp124Glu)	CKLF, CKLF-CMTM1 (D124E +3 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 2588096	NM_052999.4(CMTM1):c.398T>C (p.Phe133Ser)	CKLF-CMTM1, CMTM1 (F133S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541433	NM_052999.4(CMTM1):c.256C>G (p.Pro86Ala)	CKLF-CMTM1, CMTM1 (P86A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2530938	NM_052999.4(CMTM1):c.375G>T (p.Arg125Ser)	CKLF-CMTM1, CMTM1 (R125S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2520596	NM_052999.4(CMTM1):c.13C>T (p.His5Tyr)	CKLF-CMTM1, CMTM1 (H5Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2492220	NM_052999.4(CMTM1):c.283A>G (p.Thr95Ala)	CKLF-CMTM1, CMTM1 (T95A)	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 2406921	NM_052999.4(CMTM1):c.179G>C (p.Ser60Thr)	CKLF-CMTM1, CMTM1 (S60T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2401112	NM_052999.4(CMTM1):c.259C>T (p.Pro87Ser)	CKLF-CMTM1, CMTM1 (P87S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396471	NM_016951.4(CKLF):c.308C>A (p.Thr103Asn)	CKLF, CKLF-CMTM1 (T103N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2359380	NM_052999.4(CMTM1):c.86G>A (p.Ser29Asn)	CKLF-CMTM1, CMTM1 (S29N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2347906	NM_052999.4(CMTM1):c.196G>A (p.Ala66Thr)	CKLF-CMTM1, CMTM1 (A66T)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2321830	NM_052999.4(CMTM1):c.553C>G (p.Leu185Val)	CKLF-CMTM1, CMTM1 (L185V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2296634	NM_052999.4(CMTM1):c.163G>A (p.Ala55Thr)	CKLF-CMTM1, CMTM1 (A55T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2292613	NM_052999.4(CMTM1):c.175C>T (p.Arg59Cys)	CKLF-CMTM1, CMTM1 (R59C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2276843	NM_016951.4(CKLF):c.338T>C (p.Phe113Ser)	CKLF, CKLF-CMTM1 (F28S +3 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2235448	NM_016951.4(CKLF):c.286G>A (p.Val96Met)	CKLF, CKLF-CMTM1 (V43M +1 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 782141	NM_016951.4(CKLF):c.435G>A (p.Val145=)	CKLF, CKLF-CMTM1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
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 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: 56