ClinVar for Gene (Select 90485) - ClinVar

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Links from Gene

Items: 73

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3341632	NM_001005850.3(ZNF835):c.987A>G (p.Thr329=)	ZNF835	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 3259731	NM_001005850.3(ZNF835):c.923G>T (p.Cys308Phe)	ZNF835 (C308F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259730	NM_001005850.3(ZNF835):c.885G>C (p.Gln295His)	ZNF835 (Q295H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3259728	NM_001005850.3(ZNF835):c.973C>G (p.Arg325Gly)	ZNF835 (R325G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198714	NM_001005850.3(ZNF835):c.841G>A (p.Gly281Ser)	ZNF835 (G281S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198713	NM_001005850.3(ZNF835):c.650C>T (p.Thr217Met)	ZNF835 (T217M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198712	NM_001005850.3(ZNF835):c.592G>T (p.Asp198Tyr)	ZNF835 (D198Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198711	NM_001005850.3(ZNF835):c.424G>A (p.Glu142Lys)	ZNF835 (E142K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198710	NM_001005850.3(ZNF835):c.281A>G (p.His94Arg)	ZNF835 (H94R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198709	NM_001005850.3(ZNF835):c.25C>A (p.Leu9Ile)	ZNF835 (L9I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198708	NM_001005850.3(ZNF835):c.1295C>T (p.Ser432Leu)	ZNF835 (S432L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198707	NM_001005850.3(ZNF835):c.1204G>T (p.Val402Leu)	ZNF835 (V402L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198706	NM_001005850.3(ZNF835):c.1115G>C (p.Ser372Thr)	ZNF835 (S372T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3198705	NM_001005850.3(ZNF835):c.1093C>T (p.His365Tyr)	ZNF835 (H365Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062375	GRCh37/hg19 19q13.42-13.43(chr19:56080158-57672397)x1	CCDC106, DUXA +36 more	Copy number loss	not specified	GUncertain significance
Select item 2684894	GRCh37/hg19 19q13.43(chr19:56949121-57419586)x3	PEG3, SMIM17 +8 more	Copy number gain	not provided	GUncertain significance
Select item 2684892	GRCh37/hg19 19q13.33-13.43(chr19:49625130-57647352)x3	ACP4, ADM5 +261 more	Copy number gain	not provided	GLikely pathogenic
Select item 2595348	NM_001005850.3(ZNF835):c.1261G>C (p.Gly421Arg)	ZNF835 (G421R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592388	NM_001005850.3(ZNF835):c.636C>G (p.His212Gln)	ZNF835 (H212Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2556271	NM_001005850.3(ZNF835):c.247T>C (p.Cys83Arg)	ZNF835 (C83R)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2556044	NM_001005850.3(ZNF835):c.307G>A (p.Gly103Ser)	ZNF835 (G103S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2539494	NM_001005850.3(ZNF835):c.556C>A (p.Arg186Ser)	ZNF835 (R186S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513882	NM_001005850.3(ZNF835):c.229G>A (p.Asp77Asn)	ZNF835 (D77N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2495307	NM_001005850.3(ZNF835):c.883C>A (p.Gln295Lys)	ZNF835 (Q295K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2481261	NM_001005850.3(ZNF835):c.972C>G (p.His324Gln)	ZNF835 (H324Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464996	NM_001005850.3(ZNF835):c.90C>A (p.Asn30Lys)	ZNF835 (N30K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2411851	NM_001005850.3(ZNF835):c.1264G>A (p.Glu422Lys)	ZNF835 (E422K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2409866	NM_001005850.3(ZNF835):c.7G>A (p.Gly3Arg)	ZNF835 (G3R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2390249	NM_001005850.3(ZNF835):c.202G>A (p.Ala68Thr)	ZNF835 (A68T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2381450	NM_001005850.3(ZNF835):c.1241G>T (p.Gly414Val)	ZNF835 (G414V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2381425	NM_001005850.3(ZNF835):c.1240G>A (p.Gly414Arg)	ZNF835 (G414R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379355	NM_001005850.3(ZNF835):c.617T>C (p.Val206Ala)	ZNF835 (V206A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355754	NM_001005850.3(ZNF835):c.1114A>G (p.Ser372Gly)	ZNF835 (S372G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2346931	NM_001005850.3(ZNF835):c.1069A>G (p.Thr357Ala)	ZNF835 (T357A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339976	NM_001005850.3(ZNF835):c.61G>A (p.Glu21Lys)	ZNF835 (E21K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2339531	NM_001005850.3(ZNF835):c.404A>C (p.Glu135Ala)	ZNF835 (E135A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275294	NM_001005850.3(ZNF835):c.1322C>T (p.Thr441Met)	ZNF835 (T441M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272765	NM_001005850.3(ZNF835):c.1027T>G (p.Phe343Val)	ZNF835 (F343V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2262236	NM_001005850.3(ZNF835):c.542T>G (p.Leu181Arg)	ZNF835 (L181R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2253915	NM_001005850.3(ZNF835):c.510G>C (p.Glu170Asp)	ZNF835 (E170D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2252570	NM_001005850.3(ZNF835):c.22G>A (p.Ala8Thr)	ZNF835 (A8T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222938	NM_001005850.3(ZNF835):c.401G>A (p.Gly134Glu)	ZNF835 (G134E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2222102	NM_001005850.3(ZNF835):c.1592C>T (p.Pro531Leu)	ZNF835 (P531L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2218533	NM_001005850.3(ZNF835):c.820G>A (p.Glu274Lys)	ZNF835 (E274K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2207630	NM_001005850.3(ZNF835):c.382C>G (p.His128Asp)	ZNF835 (H128D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1526673	GRCh37/hg19 19q13.43(chr19:57136208-57478257)	PEG3, SMIM17 +3 more	Copy number gain	not specified	GUncertain significance
Select item 816096	GRCh37/hg19 19q13.43(chr19:56788816-57277655)x3	SMIM17, ZNF71 +8 more	Copy number gain	not provided	GLikely benign
Select item 564606	GRCh37/hg19 19q13.42-13.43(chr19:54196216-58759679)x3	ZNF548, ZNF549 +157 more	Copy number gain	not provided	GPathogenic
Select item 564598	GRCh37/hg19 19q13.43(chr19:56565455-57401997)x1	ZNF667, ZNF471 +16 more	Copy number loss	not provided	GUncertain significance
Select item 443658	GRCh37/hg19 19q13.42-13.43(chr19:55844155-57408007)x3	CCDC106, COX6B2 +47 more	Copy number gain	See cases	GUncertain significance
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 443202	GRCh37/hg19 19q13.42-13.43(chr19:55549385-57489784)x3	BRSK1, CCDC106 +61 more	Copy number gain	See cases	GUncertain significance
Select item 442403	GRCh37/hg19 19q13.43(chr19:56706500-58956888)x3	A1BG, AURKC +64 more	Copy number gain	See cases	GUncertain significance
Select item 442366	GRCh37/hg19 19q13.42-13.43(chr19:56212463-57191708)x3	GALP, NLRP11 +21 more	Copy number gain	See cases	GUncertain significance
Select item 394342	GRCh37/hg19 19q13.33-13.43(chr19:50489390-59095359)x3	A1BG, ACP4 +280 more	Copy number gain	See cases	GPathogenic
Select item 394098	GRCh37/hg19 19q13.43(chr19:56874577-57183789)x3	SMIM17, ZFP28 +8 more	Copy number gain	See cases	GUncertain significance
Select item 221405	GRCh37/hg19 19q13.42-13.43(chr19:56200298-57654005)x1	NLRP5, NLRP8 +26 more	Copy number loss	Breast ductal adenocarcinoma	GUncertain significance
Select item 221354	chr19:56133299..57648277 complex variant	NLRP4, CCDC106 +31 more	Complex	Breast ductal adenocarcinoma	GUncertain significance
Select item 154108	GRCh38/hg38 19q13.42-13.43(chr19:55037146-56982033)x3	BRSK1, C19orf85 +196 more	Copy number gain	See cases	GUncertain significance
Select item 153721	GRCh38/hg38 19q13.41-13.43(chr19:52143873-58445521)x3	A1BG, A1BG-AS1 +547 more	Copy number gain	See cases	GPathogenic
Select item 153557	GRCh38/hg38 19q13.43(chr19:56353449-58445521)x3	A1BG, A1BG-AS1 +179 more	Copy number gain	See cases	GUncertain significance
Select item 149081	GRCh38/hg38 19q13.42-13.43(chr19:55048514-56972458)x3	BRSK1, C19orf85 +194 more	Copy number gain	See cases	GLikely pathogenic
Select item 146579	GRCh38/hg38 19q13.33-13.43(chr19:50152520-58581203)x3	OSCAR, PEG3 +782 more	Copy number gain	See cases	GPathogenic
Select item 145961	GRCh38/hg38 19q13.42-13.43(chr19:55550939-57031576)x1	CCDC106, EDDM13 +106 more	Copy number loss	See cases	GLikely pathogenic
Select item 144762	GRCh38/hg38 19q13.41-13.43(chr19:52612432-58581203)x3	SSC5D, SYT5 +553 more	Copy number gain	See cases	GPathogenic
Select item 144709	GRCh38/hg38 19q13.41-13.43(chr19:52955056-58581203)x3	TMC4, TMEM150B +537 more	Copy number gain	See cases	GPathogenic
Select item 59128	GRCh38/hg38 19q13.43(chr19:56363208-58581203)x3	A1BG, A1BG-AS1 +215 more	Copy number gain	See cases	GPathogenic
Select item 59127	GRCh38/hg38 19q13.41-13.43(chr19:51141518-58539965)x3	A1BG, A1BG-AS1 +647 more	Copy number gain	See cases	GPathogenic
Select item 59126	GRCh38/hg38 19q13.33-13.43(chr19:49907832-58557889)x3	LOC130065082, LOC130065083 +806 more	Copy number gain	See cases	GPathogenic
Select item 59117	GRCh38/hg38 19q13.33-13.43(chr19:47929575-58572206)x3	LOC130064903, LOC130064904 +1093 more	Copy number gain	See cases	GPathogenic
Select item 59116	GRCh38/hg38 19q13.33-13.43(chr19:47908540-58539965)x3	LOC130064925, LOC130064926 +1081 more	Copy number gain	See cases	GPathogenic
Select item 57219	GRCh38/hg38 19q13.33-13.43(chr19:50191219-58535818)x3	LOC130065034, LOC130065035 +761 more	Copy number gain	See cases	GPathogenic

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Links from Gene

Items: 73