434[Gene ID] - ClinVar

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Items: 31

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 146596	GRCh38/hg38 20p13-q13.33(chr20:99557-64277321)x3	JPH2, KAT14 +2522 more	Copy number gain	See cases	GPathogenic
Select item 59195	GRCh38/hg38 20p12.2-q12(chr20:9811433-39316956)x3	LOC613266, MACROD2 +950 more	Copy number gain	See cases	GPathogenic
Select item 153447	GRCh38/hg38 20q11.21-11.23(chr20:32062768-35906606)x3	ACSS2, ACTL10 +254 more	Copy number gain	See cases	GPathogenic
Select item 146117	GRCh38/hg38 20q11.21-11.23(chr20:33432363-36821881)x1	AAR2, ACSS2 +214 more	Copy number loss	See cases	GPathogenic
Select item 3248564	NC_000020.11:g.34210141_34393539dup	AHCY, ASIP +12 more	Duplication	Obesity and hypopigmentation	GPathogenic
Select item 3130388	NM_001672.3(ASIP):c.116A>T (p.Asn39Ile)	AHCY, ASIP (N39I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242405	NM_001672.3(ASIP):c.124G>T (p.Val42Leu)	AHCY, ASIP (V42L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374309	NM_001672.3(ASIP):c.134T>C (p.Leu45Pro)	AHCY, ASIP (L45P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230217	NM_001672.3(ASIP):c.181C>A (p.Gln61Lys)	AHCY, ASIP (Q61K)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3130389	NM_001672.3(ASIP):c.185T>A (p.Ile62Asn)	AHCY, ASIP (I62N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2334266	NM_001672.3(ASIP):c.223A>G (p.Lys75Glu)	AHCY, ASIP (K75E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3318239	NM_001672.3(ASIP):c.245T>C (p.Val82Ala)	AHCY, ASIP (V82A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 775119	NM_001672.3(ASIP):c.264C>A (p.Pro88=)	AHCY, ASIP	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3130390	NM_001672.3(ASIP):c.297C>G (p.Ser99Arg)	AHCY, ASIP (S99R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 9308	NM_001672.3(ASIP):c.*25A>G	AHCY, ASIP	Single nucleotide variant (3 prime UTR variant)	SKIN/HAIR/EYE PIGMENTATION 9, DARK/LIGHT HAIR	Gassociation
Select item 3248297	NC_000020.10:g.(?_31571600)_(33001705_?)del	ACTL10, AHCY +22 more	Deletion	Hypermethioninemia with deficiency of S-adenosylhomocysteine hydrolase	GPathogenic
Select item 3248260	NC_000020.10:g.(?_31368130)_(34287210_?)del	ASIP, ACSS2 +51 more	Deletion	Glutathione synthetase deficiency with 5-oxoprolinuria	GPathogenic
Select item 1809278	GRCh37/hg19 20q11.21-11.23(chr20:29652122-35603726)x3	AAR2, ACSS2 +98 more	Copy number gain	not provided	GLikely pathogenic
Select item 1808687	GRCh37/hg19 20q11.21-11.23(chr20:29833535-34815537)x3	ACSS2, ACTL10 +86 more	Copy number gain	not provided	GLikely pathogenic
Select item 1526690	GRCh37/hg19 20p11.21-q11.22(chr20:25442597-33761550)	ACSS2, ACTL10 +71 more	Copy number gain	not specified	GPathogenic
Select item 1457888	NC_000020.10:g.(?_31189994)_(34287210_?)del	ACSS2, ACTL10 +53 more	Deletion	not provided	GPathogenic
Select item 1341087	GRCh37/hg19 20p11.23-q11.22(chr20:18665879-33903216)x3	ABHD12, ACSS1 +117 more	Copy number gain	not provided	GLikely pathogenic
Select item 816125	GRCh37/hg19 20q11.21-11.22(chr20:31966407-33169058)x3	PIGU, E2F1 +16 more	Copy number gain	not provided	GUncertain significance
Select item 689044	GRCh37/hg19 20q11.21-11.23(chr20:29833608-35087952)x3	AAR2, ACSS2 +88 more	Copy number gain	not provided	GPathogenic
Select item 635773	GRCh37/hg19 20q11.22(chr20:32854720-32914371)x3	ASIP, AHCY	Copy number gain	Intellectual disability	GUncertain significance
Select item 584348	NC_000020.10:g.(?_31996293)_(33338342_?)del	ASIP, C20orf144 +17 more	Deletion	Long QT syndrome	GUncertain significance
Select item 583982	NC_000020.10:g.(?_31996293)_(33761838_?)del	MAP1LC3A, MIR499A +25 more	Deletion	Long QT syndrome	GUncertain significance
Select item 564635	GRCh37/hg19 20q11.22(chr20:32436483-33276757)x3	ITCH, AHCY +7 more	Copy number gain	not provided	GLikely benign
Select item 443340	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)x3	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 443339	GRCh37/hg19 20p13-q13.33(chr20:61569-62915555)	AAR2, ABHD12 +540 more	Copy number gain	See cases	GPathogenic
Select item 442696	GRCh37/hg19 20q11.22(chr20:32815819-33046013)x4	AHCY, ASIP +1 more	Copy number gain	See cases	GUncertain significance

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Items: 31