DERPC[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 155358	GRCh38/hg38 16q12.2-24.3(chr16:52899183-90088654)x3	MIR138-2, MIR140 +1738 more	Copy number gain	See cases	GPathogenic
Select item 58630	GRCh38/hg38 16q13-22.2(chr16:56883592-71279975)x3	LOC130059330, LOC130059331 +599 more	Copy number gain	See cases	GPathogenic
Select item 58632	GRCh38/hg38 16q21-23.1(chr16:58456122-74708723)x3	LOC130059197, LOC130059198 +575 more	Copy number gain	See cases	GPathogenic
Select item 146601	GRCh38/hg38 16q21-24.1(chr16:62925929-84585795)x3	AARS1, ACD +939 more	Copy number gain	See cases	GPathogenic
Select item 154511	GRCh38/hg38 16q21-24.3(chr16:64389378-90081985)x3	LOC130059829, LOC130059830 +1429 more	Copy number gain	See cases	GPathogenic
Select item 58645	GRCh38/hg38 16q21-24.3(chr16:65313395-90081985)x3	LOC108281164, LOC109029536 +1426 more	Copy number gain	See cases	GPathogenic
Select item 150599	GRCh38/hg38 16q21-24.3(chr16:65511483-90096995)x3	LOC130059834, LOC130059835 +1424 more	Copy number gain	See cases	GPathogenic
Select item 155675	GRCh38/hg38 16q21-23.3(chr16:65957829-83611443)x3	LOC130059420, LOC130059421 +869 more	Copy number gain	See cases	GPathogenic
Select item 59495	GRCh38/hg38 16q22.1-23.1(chr16:68698941-74353205)x1	AARS1, AP1G1 +263 more	Copy number loss	See cases	GPathogenic
Select item 147207	GRCh38/hg38 16q22.1(chr16:68937032-69254118)x3	CHTF8, DERPC +9 more	Copy number gain	See cases	GUncertain significance
Select item 153758	GRCh38/hg38 16q22.1-23.3(chr16:69053457-83274681)x3	LOC132090408, LOC132090409 +572 more	Copy number gain	See cases	GPathogenic
Select item 2646666	NM_001002847.4(DERPC):c.1189A>C (p.Thr397Pro)	CHTF8, DERPC (T397P)	Single nucleotide variant (missense variant +2 more)	not provided	GLikely benign
Select item 2646667	NM_001002847.4(DERPC):c.819C>T (p.Leu273=)	CHTF8, DERPC	Single nucleotide variant (synonymous variant +2 more)	not provided	GLikely benign
Select item 2362922	NM_001039690.5(CHTF8):c.325C>T (p.Arg109Cys)	CHTF8, DERPC (R109C)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3267291	NM_001039690.5(CHTF8):c.320A>C (p.Lys107Thr)	CHTF8, DERPC (K107T)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2331779	NM_001039690.5(CHTF8):c.277C>T (p.Arg93Trp)	CHTF8, DERPC (R93W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2224865	NM_001039690.5(CHTF8):c.263G>A (p.Arg88His)	CHTF8, DERPC (R88H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2211031	NM_001039690.5(CHTF8):c.262C>A (p.Arg88Ser)	CHTF8, DERPC (R88S)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144854	NM_001039690.5(CHTF8):c.201G>C (p.Glu67Asp)	CHTF8, DERPC (E67D)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2476819	NM_001039690.5(CHTF8):c.178T>C (p.Tyr60His)	CHTF8, DERPC (Y60H)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3144855	NM_001039690.5(CHTF8):c.98G>A (p.Gly33Glu)	CHTF8, DERPC (G33E)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2330133	NM_001039690.5(CHTF8):c.85C>T (p.Arg29Cys)	CHTF8, DERPC (R29C)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance
Select item 2330132	NM_001039690.5(CHTF8):c.83C>T (p.Ala28Val)	CHTF8, DERPC (A28V)	Single nucleotide variant (5 prime UTR variant +2 more)	not specified	GUncertain significance

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Items: 23