ANAPC11[gene] - ClinVar

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58703	GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	MIR636, MIR6516 +1033 more	Copy number gain	See cases	GPathogenic
Select item 155275	GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	AANAT, AATK +1013 more	Copy number gain	See cases	GPathogenic
Select item 57076	GRCh38/hg38 17q25.3(chr17:78092236-83086677)x3	AATK, ACTG1 +513 more	Copy number gain	See cases	GPathogenic
Select item 57263	GRCh38/hg38 17q25.3(chr17:78901959-83086677)x3	AATK, ACTG1 +387 more	Copy number gain	See cases	GPathogenic
Select item 58714	GRCh38/hg38 17q25.3(chr17:78918650-83021095)x3	AATK, ACTG1 +385 more	Copy number gain	See cases	GPathogenic
Select item 149717	GRCh38/hg38 17q25.3(chr17:81008196-83102584)x3	AATK, ACTG1 +262 more	Copy number gain	See cases	GPathogenic
Select item 153720	GRCh38/hg38 17q25.3(chr17:81401966-83084062)x1	ACTG1, ALYREF +226 more	Copy number loss	See cases	GLikely pathogenic
Select item 154540	GRCh38/hg38 17q25.3(chr17:81859688-82017612)x1	ALYREF, ANAPC11 +40 more	Copy number loss	See cases	GBenign
Select item 145073	GRCh38/hg38 17q25.3(chr17:81871533-81891511)x4	ALYREF, ANAPC11 +4 more	Copy number gain	See cases	GBenign
Select item 60175	GRCh38/hg38 17q25.3(chr17:81885863-82358856)x3	LOC130062008, LOC130062009 +95 more	Copy number gain	See cases	GUncertain significance
Select item 3350262	NM_005782.4(ALYREF):c.46C>T (p.Leu16=)	ALYREF, ANAPC11	Single nucleotide variant (synonymous variant +2 more)	ALYREF-related disorder	GLikely benign
Select item 2279903	NM_005782.4(ALYREF):c.11C>T (p.Ser4Phe)	ALYREF, ANAPC11 (S4F)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2636880	NM_005782.4(ALYREF):c.5C>A (p.Pro2His)	ALYREF, ANAPC11 (P2H)	Single nucleotide variant (missense variant +2 more)	ALYREF-related disorder	GUncertain significance
Select item 3293800	NM_001002248.3(ANAPC11):c.31G>A (p.Val11Met)	ANAPC11 (V11M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2471429	NM_001002248.3(ANAPC11):c.110-657T>C	ANAPC11 (I44T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117730	NM_001002248.3(ANAPC11):c.110-616C>G	ANAPC11 (L58V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293818	NM_001002248.3(ANAPC11):c.110-453C>T	ANAPC11 (P112L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117731	NM_001002248.3(ANAPC11):c.153C>T (p.Cys51=)	ANAPC11 (A80V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3117733	NM_001002248.3(ANAPC11):c.196G>A (p.Ala66Thr)	ANAPC11 (A66T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3293811	NM_001002248.3(ANAPC11):c.248A>G (p.Lys83Arg)	ANAPC11 (R112G +1 more)	Single nucleotide variant (synonymous variant +1 more)	not specified	GLikely benign
Select item 3243134	NC_000017.10:g.(?_79477716)_(80901020_?)dup	ACTG1, ALYREF +52 more	Duplication	not provided	GUncertain significance
Select item 2685609	GRCh37/hg19 17q25.3(chr17:79128754-80092824)x1	AATK, ACTG1 +41 more	Copy number loss	not provided	GLikely pathogenic
Select item 2445210	Single allele	FOXK2, GCGR +51 more	Deletion	See cases	GPathogenic
Select item 2425656	NC_000017.10:g.(?_79618104)_(79894690_?)dup	ALYREF, ANAPC11 +17 more	Duplication	not provided	GUncertain significance
Select item 2424500	NC_000017.10:g.(?_79477716)_(80900339_?)dup	ACTG1, ALYREF +52 more	Duplication	not provided	GUncertain significance
Select item 1701331	GRCh37/hg19 17q25.1-25.3(chr17:73481509-81043199)x3	EVPL, EXOC7 +146 more	Copy number gain	not provided	GPathogenic
Select item 689209	GRCh37/hg19 17q24.1-25.3(chr17:62778720-81041938)x3	AANAT, AATK +226 more	Copy number gain	not provided	GPathogenic
Select item 687727	GRCh37/hg19 17q25.3(chr17:78608912-81041938)x3	AATK, ACTG1 +65 more	Copy number gain	not provided	GPathogenic
Select item 687520	GRCh37/hg19 17q25.3(chr17:79663313-80197463)x3	ALYREF, ANAPC11 +26 more	Copy number gain	not provided	GUncertain significance
Select item 564476	GRCh37/hg19 17q25.3(chr17:76552611-81041938)x3	AATK, ACTG1 +88 more	Copy number gain	not provided	GLikely pathogenic
Select item 564463	GRCh37/hg19 17q24.1-25.3(chr17:63689671-81041938)x3	AANAT, AATK +222 more	Copy number gain	not provided	GPathogenic
Select item 443488	GRCh37/hg19 17q24.2-25.3(chr17:67002415-81041938)x3	AANAT, AATK +202 more	Copy number gain	See cases	GPathogenic
Select item 443446	GRCh37/hg19 17q25.1-25.3(chr17:73951701-81041938)x3	AANAT, AATK +128 more	Copy number gain	See cases	GPathogenic
Select item 441816	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)x3	ALOX12, ALOX12B +1143 more	Copy number gain	See cases	GPathogenic
Select item 441815	GRCh37/hg19 17p13.3-q25.3(chr17:526-81041938)	SPEM2, TBCD +1143 more	Copy number gain	See cases	GPathogenic
Select item 395646	GRCh37/hg19 17q21.31-25.3(chr17:42580684-81085615)x3	AANAT, AATK +458 more	Copy number gain	See cases	GPathogenic

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Items: 36