CLPSL2[gene] - ClinVar - NCBI

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Items: 16

	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 2389018	NM_207409.4(CLPSL2):c.55C>T (p.Leu19Phe)	CLPSL2, LOC129996259 (L19F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3267843	NM_207409.4(CLPSL2):c.106C>T (p.His36Tyr)	CLPSL2 (H36Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2529080	NM_207409.4(CLPSL2):c.124A>G (p.Ser42Gly)	CLPSL2 (S42G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2550564	NM_207409.4(CLPSL2):c.224A>G (p.Asn75Ser)	CLPSL2 (N75S)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2412283	NM_207409.4(CLPSL2):c.241C>T (p.Arg81Trp)	CLPSL2 (P107L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2393626	NM_207409.4(CLPSL2):c.254C>T (p.Thr85Met)	CLPSL2 (T85M)	Single nucleotide variant (synonymous variant +2 more)	not specified	GUncertain significance
Select item 2319126	NM_207409.4(CLPSL2):c.283C>T (p.Arg95Cys)	CLPSL2 (P121L +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2685202	GRCh37/hg19 6p21.31-21.1(chr6:35562152-42003452)x1	BNIP5, APOBEC2 +67 more	Copy number loss	not provided	GPathogenic
Select item 2445505	NC_000006.11:g.(?_32148920)_(36953949_?)dup	ARMC12, BRPF3 +94 more	Duplication	not provided	GUncertain significance
Select item 2427350	NC_000006.11:g.(?_30695893)_(36953949_?)dup	ABHD16A, AGER +172 more	Duplication	Proteasome-associated autoinflammatory syndrome 1	GUncertain significance
Select item 997072	GRCh37/hg19 6p21.31-21.2(chr6:34401304-38435497)	ANKS1A, ARMC12 +49 more	Copy number loss	Severe intrauterine growth retardation	GPathogenic
Select item 625706	GRCh37/hg19 6p22.1-q14.1(chr6:29455465-81447367)	ERVH-3, ETV7 +427 more	Copy number gain	not provided	GPathogenic
Select item 563171	GRCh37/hg19 6p21.31-21.2(chr6:34683518-36905281)x3	UHRF1BP1, SRSF3 +34 more	Copy number gain	not provided	GLikely pathogenic
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