LOC129929491[gene] - ClinVar

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Search results

Items: 27

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2664871	GRCh38/hg38 1p36.33-35.1(chr1:99125-34026935)x3	A2ML1-AS2, A3GALT2 +2151 more	Copy number gain	Trisomy 12p	GPathogenic
Select item 59846	GRCh38/hg38 1p36.32-36.13(chr1:3006193-17688934)x1	LINC02783, LINC03126 +804 more	Copy number loss	See cases	GPathogenic
Select item 154704	GRCh38/hg38 1p36.31-36.13(chr1:5363826-18360302)x1	PLOD1, PRAMEF1 +730 more	Copy number loss	See cases	GPathogenic
Select item 148885	GRCh38/hg38 1p36.31-36.21(chr1:6303641-15799093)x1	LOC129929327, LOC129929328 +557 more	Copy number loss	See cases	GPathogenic
Select item 154839	GRCh38/hg38 1p36.31-36.13(chr1:6554885-16056011)x3	AADACL3, AADACL4 +563 more	Copy number gain	See cases	GPathogenic
Select item 59885	GRCh38/hg38 1p36.23-36.13(chr1:9034671-16441465)x1	AADACL3, AADACL4 +462 more	Copy number loss	See cases	GPathogenic
Select item 152293	GRCh38/hg38 1p36.22-36.21(chr1:9428538-15815791)x1	AADACL3, AADACL4 +370 more	Copy number loss	See cases	GPathogenic
Select item 1707471	NC_000001.11:g.10115497_16283149dup	LOC110120623, LOC110120648 +361 more	Duplication	not specified	GLikely pathogenic
Select item 152937	GRCh38/hg38 1p36.22-36.21(chr1:10264397-15780840)x1	AADACL3, AADACL4 +304 more	Copy number loss	See cases	GPathogenic
Select item 59892	GRCh38/hg38 1p36.22-36.13(chr1:10621776-16520709)x1	AADACL3, AADACL4 +337 more	Copy number loss	See cases	GPathogenic
Select item 59894	GRCh38/hg38 1p36.22-36.13(chr1:10809039-16422500)x1	LOC112577504, LOC112577505 +316 more	Copy number loss	See cases	GPathogenic
Select item 59895	GRCh38/hg38 1p36.22-36.13(chr1:11121625-16324498)x1	AADACL3, AADACL4 +288 more	Copy number loss	See cases	GPathogenic
Select item 148652	GRCh38/hg38 1p36.21-36.13(chr1:12724785-16034788)x1	AADACL3, AGMAT +151 more	Copy number loss	See cases	GPathogenic
Select item 58056	GRCh38/hg38 1p36.21-36.13(chr1:13619979-18466172)x3	LOC129929515, LOC129929516 +211 more	Copy number gain	See cases	GPathogenic
Select item 146292	GRCh38/hg38 1p36.21-36.13(chr1:15052047-16499873)x1	AGMAT, ARHGEF19 +112 more	Copy number loss	See cases	GLikely pathogenic
Select item 57443	GRCh38/hg38 1p36.21-36.12(chr1:15385267-20980349)x1	ACTL8, AGMAT +303 more	Copy number loss	See cases	GPathogenic
Select item 2534153	NM_024758.5(AGMAT):c.220G>T (p.Ala74Ser)	AGMAT, LOC129929491 (A74S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095969	NM_024758.5(AGMAT):c.195G>T (p.Gln65His)	AGMAT, LOC129929491 (Q65H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095966	NM_024758.5(AGMAT):c.175A>G (p.Met59Val)	AGMAT, LOC129929491 (M59V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355729	NM_024758.5(AGMAT):c.137G>A (p.Ser46Asn)	AGMAT, LOC129929491 (S46N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276058	NM_024758.5(AGMAT):c.105G>C (p.Gln35His)	AGMAT, LOC129929491 (Q35H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2238958	NM_024758.5(AGMAT):c.100C>T (p.Arg34Cys)	AGMAT, LOC129929491 (R34C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2597588	NM_024758.5(AGMAT):c.91C>T (p.Arg31Cys)	AGMAT, LOC129929491 (R31C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2319891	NM_024758.5(AGMAT):c.82C>G (p.Pro28Ala)	AGMAT, LOC129929491 (P28A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 784932	NM_024758.5(AGMAT):c.30C>T (p.Ala10=)	AGMAT, LOC129929491	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2352507	NM_024758.5(AGMAT):c.28G>T (p.Ala10Ser)	AGMAT, LOC129929491 (A10S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3095961	NM_024758.5(AGMAT):c.11T>G (p.Leu4Arg)	AGMAT, LOC129929491 (L4R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 27