MIS12[gene] - ClinVar

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Items: 38

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 154089	GRCh38/hg38 17p13.3-12(chr17:150732-14764202)x3	ABR, ABR-AS1 +962 more	Copy number gain	See cases	GPathogenic
Select item 153177	GRCh38/hg38 17p13.3-13.2(chr17:150732-5935377)x1	ABR, ABR-AS1 +463 more	Copy number loss	See cases	GPathogenic
Select item 149531	GRCh38/hg38 17p13.3-12(chr17:162016-12343901)x3	LOC130059883, LOC130059884 +922 more	Copy number gain	See cases	GPathogenic
Select item 149158	GRCh38/hg38 17p13.3-13.1(chr17:162016-7697012)x1	TRARG1, TRPV1 +651 more	Copy number loss	See cases	GPathogenic
Select item 144699	GRCh38/hg38 17p13.3-13.1(chr17:162088-6959050)x1	ABR, ABR-AS1 +498 more	Copy number loss	See cases	GPathogenic
Select item 2579287	GRCh38/hg38 17p13.3-12(chr17:165730-11404096)x3	SAT2, SCARF1 +911 more	Copy number gain	Chromosome 17p13.3 duplication syndrome	GPathogenic
Select item 59542	GRCh38/hg38 17p13.3-13.2(chr17:193307-5652222)x1	LOC121848004, LOC121848005 +457 more	Copy number loss	See cases	GPathogenic
Select item 145642	GRCh38/hg38 17p13.3-13.1(chr17:198748-7491129)x3	LOC130059937, LOC130059938 +604 more	Copy number gain	See cases	GPathogenic
Select item 59563	GRCh38/hg38 17p13.2-13.1(chr17:3601515-7178024)x1	AIPL1, ALOX12 +290 more	Copy number loss	See cases	GPathogenic
Select item 146235	GRCh38/hg38 17p13.2(chr17:4044302-5943772)x1	ALOX15, ANKFY1 +166 more	Copy number loss	See cases	GLikely pathogenic
Select item 153939	GRCh38/hg38 17p13.2(chr17:5252176-5761432)x3	C1QBP, DERL2 +22 more	Copy number gain	See cases	GUncertain significance
Select item 145540	GRCh38/hg38 17p13.2(chr17:5385377-5943772)x3	C1QBP, DERL2 +23 more	Copy number gain	See cases	GUncertain significance
Select item 2245336	NM_001258217.2(MIS12):c.23A>G (p.Tyr8Cys)	MIS12 (Y8C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525628	NM_001258217.2(MIS12):c.68G>A (p.Arg23Gln)	MIS12 (R23Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3126712	NM_001258217.2(MIS12):c.78T>G (p.Ile26Met)	MIS12 (I26M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2402122	NM_001258217.2(MIS12):c.156C>G (p.Asp52Glu)	MIS12 (D52E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275993	NM_001258217.2(MIS12):c.218G>T (p.Gly73Val)	MIS12 (G73V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244535	NM_001258217.2(MIS12):c.275G>A (p.Arg92His)	MIS12 (R92H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589687	NM_001258217.2(MIS12):c.287A>T (p.Asn96Ile)	MIS12 (N96I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294941	NM_001258217.2(MIS12):c.386A>C (p.Lys129Thr)	MIS12 (K129T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2464887	NM_001258217.2(MIS12):c.448G>T (p.Ala150Ser)	MIS12 (A150S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2250404	NM_001258217.2(MIS12):c.461A>G (p.Gln154Arg)	MIS12 (Q154R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3294940	NM_001258217.2(MIS12):c.482A>T (p.Glu161Val)	MIS12 (E161V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3243205	NC_000017.10:g.(?_422368)_(8285628_?)dup	FBXO39, FGF11 +209 more	Duplication	not provided	GUncertain significance
Select item 3063503	GRCh37/hg19 17p13.2(chr17:5308495-5619495)x3	C1QBP, DERL2 +5 more	Copy number gain	not specified	GUncertain significance
Select item 3063486	GRCh37/hg19 17p13.3-11.2(chr17:525-21510992)x3	ABR, ACADVL +329 more	Copy number gain	not specified	GPathogenic
Select item 3063485	GRCh37/hg19 17p13.3-13.2(chr17:9474-6017500)x1	ABR, ALOX15 +116 more	Copy number loss	not specified	GPathogenic
Select item 2427557	NC_000017.10:g.(?_5289526)_(6616652_?)dup	AIPL1, C17orf100 +14 more	Duplication	Developmental and epileptic encephalopathy, 25	GUncertain significance
Select item 980143	GRCh37/hg19 17p13.2(chr17:5143295-5850209)x3	RABEP1, RPAIN +6 more	Copy number gain	not provided	GUncertain significance
Select item 816504	GRCh37/hg19 17p13.3-13.2(chr17:8547-5627408)x1	ABR, ALOX15 +115 more	Copy number loss	See cases	GPathogenic
Select item 815898	GRCh37/hg19 17p13.2(chr17:5378522-5692834)x3	DERL2, MIS12 +1 more	Copy number gain	not provided	GUncertain significance
Select item 688934	GRCh37/hg19 17p13.2(chr17:3759126-6128911)x1	ALOX15, ANKFY1 +48 more	Copy number loss	not provided	GUncertain significance
Select item 625578	GRCh37/hg19 17p13.3-13.2(chr17:47546-6287620)	ABR, ALOX15 +115 more	Copy number gain	Chromosome 17P13.3, telomeric, duplication syndrome	GPathogenic
Select item 564377	GRCh37/hg19 17p13.3-12(chr17:525-11186432)x3	ABR, ACADVL +240 more	Copy number gain	not provided	GPathogenic
Select item 443659	GRCh37/hg19 17p13.3-12(chr17:525-15027737)x3	ABR, ACADVL +250 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 395716	GRCh37/hg19 17p13.3-13.1(chr17:1113102-6742486)	AIPL1, ALOX15 +115 more	Copy number gain	See cases	GPathogenic

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Items: 38