ClinVar for Gene (Select 148198) - ClinVar

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Links from Gene

Items: 68

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3259893	NM_001098626.2(ZNF98):c.335A>G (p.Tyr112Cys)	ZNF98 (Y112C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259892	NM_001098626.2(ZNF98):c.1606C>T (p.His536Tyr)	ZNF98 (H536Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259891	NM_001098626.2(ZNF98):c.1511A>G (p.His504Arg)	ZNF98 (H504R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199035	NM_001098626.2(ZNF98):c.996C>G (p.Ser332Arg)	ZNF98 (S332R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199034	NM_001098626.2(ZNF98):c.97G>A (p.Ala33Thr)	ZNF98 (A33T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199033	NM_001098626.2(ZNF98):c.680C>T (p.Thr227Ile)	ZNF98 (T227I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199032	NM_001098626.2(ZNF98):c.558A>C (p.Glu186Asp)	ZNF98 (E186D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199031	NM_001098626.2(ZNF98):c.523G>A (p.Gly175Arg)	ZNF98 (G175R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3199030	NM_001098626.2(ZNF98):c.263C>A (p.Ser88Tyr)	ZNF98 (S88Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199029	NM_001098626.2(ZNF98):c.1609A>G (p.Lys537Glu)	ZNF98 (K537E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199028	NM_001098626.2(ZNF98):c.1594A>G (p.Ile532Val)	ZNF98 (I532V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199027	NM_001098626.2(ZNF98):c.1571G>A (p.Gly524Asp)	ZNF98 (G524D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199026	NM_001098626.2(ZNF98):c.1478A>G (p.Glu493Gly)	ZNF98 (E493G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3199024	NM_001098626.2(ZNF98):c.1348A>G (p.Thr450Ala)	ZNF98 (T450A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2649651	NM_001098626.2(ZNF98):c.1089C>T (p.Ser363=)	ZNF98	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649650	NM_001098626.2(ZNF98):c.1338A>C (p.Ser446=)	ZNF98	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649649	NM_001098626.2(ZNF98):c.1395A>G (p.Glu465=)	ZNF98	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2649648	NM_001098626.2(ZNF98):c.1398A>G (p.Glu466=)	ZNF98	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2624152	NM_001098626.2(ZNF98):c.1528A>G (p.Met510Val)	ZNF98 (M510V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2614582	NM_001098626.2(ZNF98):c.1612A>G (p.Met538Val)	ZNF98 (M538V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2591964	NM_001098626.2(ZNF98):c.1621A>C (p.Thr541Pro)	ZNF98 (T541P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535981	NM_001098626.2(ZNF98):c.368G>A (p.Arg123Lys)	ZNF98 (R123K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533601	NM_001098626.2(ZNF98):c.1585A>G (p.Asn529Asp)	ZNF98 (N529D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2532589	NM_001098626.2(ZNF98):c.947A>G (p.His316Arg)	ZNF98 (H316R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2511829	NM_001098626.2(ZNF98):c.746G>T (p.Arg249Leu)	ZNF98 (R249L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510321	NM_001098626.2(ZNF98):c.745C>T (p.Arg249Trp)	ZNF98 (R249W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510093	NM_001098626.2(ZNF98):c.1450C>A (p.His484Asn)	ZNF98 (H484N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494830	NM_001098626.2(ZNF98):c.1451A>G (p.His484Arg)	ZNF98 (H484R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2483949	NM_001098626.2(ZNF98):c.1034C>T (p.Thr345Ile)	ZNF98 (T345I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467686	NM_001098626.2(ZNF98):c.1649G>A (p.Ser550Asn)	ZNF98 (S550N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462697	NM_001098626.2(ZNF98):c.1081C>T (p.Arg361Trp)	ZNF98 (R361W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2458965	NM_001098626.2(ZNF98):c.1291G>A (p.Glu431Lys)	ZNF98 (E431K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396550	NM_001098626.2(ZNF98):c.1285A>T (p.Thr429Ser)	ZNF98 (T429S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2372291	NM_001098626.2(ZNF98):c.170C>T (p.Ser57Phe)	ZNF98 (S57F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2365869	NM_001098626.2(ZNF98):c.637A>G (p.Lys213Glu)	ZNF98 (K213E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2363153	NM_001098626.2(ZNF98):c.1530G>A (p.Met510Ile)	ZNF98 (M510I)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2347101	NM_001098626.2(ZNF98):c.1249C>T (p.Arg417Trp)	ZNF98 (R417W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346759	NM_001098626.2(ZNF98):c.296G>A (p.Gly99Asp)	ZNF98 (G99D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2342414	NM_001098626.2(ZNF98):c.1144G>C (p.Glu382Gln)	ZNF98 (E382Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2333620	NM_001098626.2(ZNF98):c.413G>A (p.Cys138Tyr)	ZNF98 (C138Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326194	NM_001098626.2(ZNF98):c.1004C>T (p.Ser335Leu)	ZNF98 (S335L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2318427	NM_001098626.2(ZNF98):c.16G>A (p.Gly6Arg)	ZNF98 (G6R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2310244	NM_001098626.2(ZNF98):c.1516A>G (p.Thr506Ala)	ZNF98 (T506A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2307360	NM_001098626.2(ZNF98):c.1369A>G (p.Thr457Ala)	ZNF98 (T457A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285204	NM_001098626.2(ZNF98):c.1588T>C (p.Ser530Pro)	ZNF98 (S530P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2280856	NM_001098626.2(ZNF98):c.1549C>G (p.Pro517Ala)	ZNF98 (P517A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2254729	NM_001098626.2(ZNF98):c.546C>A (p.Phe182Leu)	ZNF98 (F182L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252513	NM_001098626.2(ZNF98):c.1659T>A (p.Asn553Lys)	ZNF98 (N553K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244501	NM_001098626.2(ZNF98):c.1049A>G (p.Tyr350Cys)	ZNF98 (Y350C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2243481	NM_001098626.2(ZNF98):c.893A>C (p.Glu298Ala)	ZNF98 (E298A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242235	NM_001098626.2(ZNF98):c.1305A>T (p.Lys435Asn)	ZNF98 (K435N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2225890	NM_001098626.2(ZNF98):c.1229T>C (p.Val410Ala)	ZNF98 (V410A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207872	NM_001098626.2(ZNF98):c.1654A>G (p.Asn552Asp)	ZNF98 (N552D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1330177	GRCh37/hg19 19p13.11-q13.2(chr19:19546923-41313229)x3	ACP7, ACTMAP +255 more	Copy number gain	Specific learning disability	GPathogenic
Select item 816522	GRCh37/hg19 19p12(chr19:22208751-23199700)x3	ZNF257, ZNF492 +5 more	Copy number gain	See cases	GLikely benign
Select item 816071	GRCh37/hg19 19p12(chr19:21717186-23008275)x3	ZNF100, ZNF208 +8 more	Copy number gain	not provided	GLikely benign
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 221350	chr19:19230868-24115369 complex variant	ATP13A1, BORCS8 +49 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 153793	GRCh38/hg38 19p12(chr19:22159102-23021493)x3	LINC01233, LINC01785 +10 more	Copy number gain	See cases	GUncertain significance
Select item 152242	GRCh38/hg38 19p12(chr19:22176690-23010173)x3	LINC01233, LINC01785 +9 more	Copy number gain	See cases	GUncertain significance
Select item 147522	GRCh38/hg38 19p13.12-12(chr19:15133594-24193591)x3	ABHD8, AKAP8 +574 more	Copy number gain	See cases	GPathogenic
Select item 146475	GRCh38/hg38 19p12(chr19:21591877-22802732)x3	ZNF100, LINC01233 +13 more	Copy number gain	See cases	GUncertain significance
Select item 145763	GRCh38/hg38 19p12(chr19:21591877-22830542)x3	LINC01233, LINC01785 +14 more	Copy number gain	See cases	GBenign
Select item 145093	GRCh38/hg38 19p12(chr19:21591877-22802673)x3	LINC01233, LINC01785 +13 more	Copy number gain	See cases	GBenign
Select item 144406	GRCh38/hg38 19p13.2-q13.31(chr19:11227942-44626354)x3	ABHD8, ACP5 +2135 more	Copy number gain	See cases	GPathogenic
Select item 59114	GRCh38/hg38 19p13.12-q11(chr19:13974677-27839676)x3	ABHD8, ADGRE2 +695 more	Copy number gain	See cases	GPathogenic
Select item 57042	GRCh38/hg38 19p13.11-q13.11(chr19:17176767-34924150)x3	LOC130064154, LOC130064155 +625 more	Copy number gain	See cases	GPathogenic

ClinVar

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Links from Gene

Items: 68