FXYD3[gene] - ClinVar

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Items: 35

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 146619	GRCh38/hg38 19q12-13.13(chr19:29661858-38114723)x1	ALKBH6, ANKRD27 +459 more	Copy number loss	See cases	GPathogenic
Select item 147631	GRCh38/hg38 19q12-13.13(chr19:29671324-37902990)x1	ALKBH6, ANKRD27 +439 more	Copy number loss	See cases	GPathogenic
Select item 153499	GRCh38/hg38 19q12-13.12(chr19:31367353-35417098)x1	ANKRD27, CD22 +193 more	Copy number loss	See cases	GPathogenic
Select item 2255762	NM_005971.4(FXYD3):c.-15+983G>C	FXYD3 (G13R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2601319	NM_005971.4(FXYD3):c.-14-192C>T	FXYD3 (P26L)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2226044	NM_005971.4(FXYD3):c.-14-138A>C	FXYD3 (Q44P)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3097564	NM_005971.4(FXYD3):c.-14-135G>A	FXYD3 (R45Q)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3097565	NM_005971.4(FXYD3):c.-14-121C>T	FXYD3 (P50S)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2599068	NM_005971.4(FXYD3):c.-14-114C>T	FXYD3 (P52L)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign
Select item 2398089	NM_005971.4(FXYD3):c.-8G>T	FXYD3 (R27L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2350892	NM_005971.4(FXYD3):c.-5C>T	FXYD3 (S28F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3097566	NM_005971.4(FXYD3):c.44T>C (p.Phe15Ser)	FXYD3 (F44S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2522362	NM_005971.4(FXYD3):c.58G>A (p.Ala20Thr)	FXYD3 (A77T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334095	NM_005971.4(FXYD3):c.83G>T (p.Ser28Ile)	FXYD3 (S28I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2551193	NM_005971.4(FXYD3):c.115G>T (p.Val39Phe)	FXYD3 (V68F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489126	NM_005971.4(FXYD3):c.139G>A (p.Val47Ile)	FXYD3 (V104I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2340002	NM_005971.4(FXYD3):c.214C>T (p.His72Tyr)	FXYD3 (H101Y +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062386	GRCh37/hg19 19q11-13.2(chr19:28271146-41508851)x3	SLC7A9, SNRPA +215 more	Copy number gain	not specified	GPathogenic
Select item 2671623	Single allele	ALKBH6, APLP1 +72 more	Deletion	not provided	GPathogenic
Select item 2424426	NC_000019.9:g.(?_33167170)_(36643309_?)dup	FFAR3, FXYD1 +83 more	Duplication	Hereditary spastic paraplegia 75	GUncertain significance
Select item 1412985	NC_000019.9:g.(?_35521725)_(36643309_?)del	PSENEN, RBM42 +54 more	Deletion	Brugada syndrome 5	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 812929	Single allele	MAG, FXYD5 +33 more	Deletion	Dystonic disorder	GPathogenic
Select item 687741	GRCh37/hg19 19q13.12(chr19:35548527-35772471)x3	FAM187B, FXYD1 +7 more	Copy number gain	not provided	GUncertain significance
Select item 685279	GRCh37/hg19 19q13.12(chr19:35613953-36183886)x1	ATP4A, CD22 +24 more	Copy number loss	not provided	GUncertain significance
Select item 685025	GRCh37/hg19 19q11-13.33(chr19:28271106-49213832)x3	ACP7, ACTMAP +434 more	Copy number gain	not provided	GPathogenic
Select item 625761	GRCh37/hg19 19q13.11-13.12(chr19:35043556-36316644)	ARHGAP33, ATP4A +44 more	Copy number loss	not provided	GPathogenic
Select item 625760	GRCh37/hg19 19q13.11-13.12(chr19:35111811-37744992)	ALKBH6, APLP1 +79 more	Copy number loss	Generalized epilepsy with febrile seizures plus, type 1	GPathogenic
Select item 443499	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)	BICRA, BLOC1S3 +1364 more	Copy number gain	See cases	GPathogenic
Select item 443498	GRCh37/hg19 19p13.3-q13.43(chr19:260912-58956888)x3	A1BG, ABCA7 +1364 more	Copy number gain	See cases	GPathogenic
Select item 394699	GRCh37/hg19 19q13.12(chr19:35612084-35622065)x3	FXYD3, LGI4	Copy number gain	See cases	GUncertain significance
Select item 394109	GRCh37/hg19 19q12-13.12(chr19:30735448-36120396)x3	ANKRD27, ATP4A +58 more	Copy number gain	See cases	GPathogenic
Select item 394012	GRCh37/hg19 19q13.12(chr19:35612084-35617093)x3	FXYD3, LGI4	Copy number gain	See cases	GUncertain significance
Select item 221398	GRCh37/hg19 19q13.12(chr19:35516999-35990896)x3	CD22, DMKN +18 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance

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Items: 35