H2AC15[gene] - ClinVar

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Items: 24

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155430	GRCh38/hg38 6p25.3-12.3(chr6:156974-46789291)x3	ILRUN-AS1, IP6K3 +2582 more	Copy number gain	See cases	GPathogenic
Select item 150044	GRCh38/hg38 6p25.2-21.33(chr6:3224310-30657190)x3	ABCF1, ABT1 +1340 more	Copy number gain	See cases	GPathogenic
Select item 144210	GRCh38/hg38 6p22.2-22.1(chr6:26280579-28727313)x3	ABT1, BTN1A1 +344 more	Copy number gain	See cases	GUncertain significance
Select item 3283303	NM_003510.3(H2AC15):c.373C>T (p.His125Tyr)	H2AC15 (H125Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283302	NM_003510.3(H2AC15):c.358A>G (p.Lys120Glu)	H2AC15 (K120E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103704	NM_003510.3(H2AC15):c.334A>G (p.Ile112Val)	H2AC15 (I112V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103703	NM_003510.3(H2AC15):c.316G>A (p.Gly106Ser)	H2AC15, LOC129996140 (G106S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283301	NM_003510.3(H2AC15):c.262A>G (p.Ile88Val)	H2AC15, LOC129996140 (I88V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103702	NM_003510.3(H2AC15):c.235A>G (p.Ile79Val)	H2AC15, LOC129996140 (I79V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103701	NM_003510.3(H2AC15):c.211G>A (p.Ala71Thr)	H2AC15 (A71T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283300	NM_003510.3(H2AC15):c.203G>A (p.Gly68Asp)	H2AC15 (G68D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103700	NM_003510.3(H2AC15):c.148G>C (p.Val50Leu)	H2AC15, LOC129996141 (V50L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103699	NM_003510.3(H2AC15):c.146C>T (p.Pro49Leu)	H2AC15, LOC129996141 (P49L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3283299	NM_003510.3(H2AC15):c.136G>T (p.Ala46Ser)	H2AC15, LOC129996141 (A46S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103698	NM_003510.3(H2AC15):c.116A>G (p.Asn39Ser)	H2AC15, LOC129996141 (N39S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489983	NM_003510.3(H2AC15):c.67G>T (p.Gly23Cys)	H2AC15, LOC129996141 (G23C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103705	NM_003510.3(H2AC15):c.48G>C (p.Lys16Asn)	H2AC15 (K16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2611021	NM_003510.3(H2AC15):c.35G>A (p.Arg12His)	H2AC15 (R12H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3103706	NM_003510.3(H2AC15):c.5C>T (p.Ser2Leu)	H2AC15 (S2L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3062925	GRCh37/hg19 6p22.1(chr6:27613035-28021256)x3	H1-5, H2AC13 +17 more	Copy number gain	not specified	GUncertain significance
Select item 814806	GRCh37/hg19 6p22.1(chr6:27616157-28011557)x3	H4C12, H2AC17 +17 more	Copy number gain	not provided	GLikely benign
Select item 443497	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)	AARS2, ABCC10 +1028 more	Copy number gain	See cases	GPathogenic
Select item 443496	GRCh37/hg19 6p25.3-q27(chr6:156975-170919482)x3	RING1, RIOK1 +1028 more	Copy number gain	See cases	GPathogenic
Select item 221453	GRCh37/hg19 6p22.1(chr6:27775494-27861432)x3	H2BC13, H2BC14 +14 more	Copy number gain	Breast ductal adenocarcinoma	GUncertain significance

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Items: 24