ATP5MC2[gene] - ClinVar

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Items: 22

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 150740	GRCh38/hg38 12p13.33-q24.33(chr12:121271-133196807)x3	ACAD10, ACADS +4836 more	Copy number gain	See cases	GPathogenic
Select item 59017	GRCh38/hg38 12q13.13(chr12:53099658-53724525)x1	AAAS, AMHR2 +74 more	Copy number loss	See cases	GPathogenic
Select item 59018	GRCh38/hg38 12q13.13(chr12:53224024-54222450)x1	AAAS, AMHR2 +114 more	Copy number loss	See cases	GPathogenic
Select item 152934	GRCh38/hg38 12q13.13-13.3(chr12:53420606-56202942)x3	PMEL, PPP1R1A +219 more	Copy number gain	See cases	GPathogenic
Select item 2549485	NM_005176.7(ATP5MC2):c.376A>C (p.Met126Leu)	ATP5MC2 (M88L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532922	NM_005176.7(ATP5MC2):c.322C>G (p.Leu108Val)	ATP5MC2 (L124V +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3131705	NM_005176.7(ATP5MC2):c.269G>A (p.Gly90Glu)	ATP5MC2 (G52E +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3131704	NM_005176.7(ATP5MC2):c.205G>A (p.Asp69Asn)	ATP5MC2 (D85N +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3131703	NM_005176.7(ATP5MC2):c.191T>C (p.Ile64Thr)	ATP5MC2 (F27L +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3329376	NM_005176.7(ATP5MC2):c.126C>G (p.Ser42Arg)	ATP5MC2 (S42R +4 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3131702	NM_005176.7(ATP5MC2):c.124A>G (p.Ser42Gly)	ATP5MC2 (S4G +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2552528	NM_005176.7(ATP5MC2):c.71C>T (p.Pro24Leu)	ATP5MC2 (P24L +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2458973	NM_005176.7(ATP5MC2):c.68G>A (p.Arg23His)	ATP5MC2 (R21H +2 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3131701	NM_005176.7(ATP5MC2):c.11G>A (p.Cys4Tyr)	ATP5MC2 (C20Y +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3131700	NM_005176.7(ATP5MC2):c.-9C>T	ATP5MC2 (P14S)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3131699	NM_005176.5(ATP5MC2):c.100C>G (p.Arg34Gly)	ATP5MC2, LOC130007995 (R34G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3063260	GRCh37/hg19 12q13.13(chr12:53502510-54256094)x3	AAAS, AMHR2 +19 more	Copy number gain	not specified	GUncertain significance
Select item 635875	Single allele	AMHR2, ATF7 +26 more	Deletion	Neurodevelopmental disorder	GPathogenic
Select item 524190	NC_000012.11:g.26370251_54361538inv	BICD1, HDAC7 +212 more	Inversion	not specified	GUncertain significance
Select item 441984	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)	SLC15A5, SLC16A7 +1006 more	Copy number gain	See cases	GPathogenic
Select item 441983	GRCh37/hg19 12p13.33-q24.33(chr12:173787-133777902)x3	A2M, A2ML1 +1006 more	Copy number gain	See cases	GPathogenic
Select item 268075	GRCh37/hg19 12p13.33-q24.33(chr12:1-133851895)x3	GALNT8, H2AJ +1007 more	Copy number gain	See cases	GPathogenic

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Items: 22