ClinVar for Gene (Select 101928343) - ClinVar

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Links from Gene

Items: 21

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3140520	NM_181449.3(CD300E):c.529G>A (p.Val177Met)	CD300E, LOC101928343 (V177M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140519	NM_181449.3(CD300E):c.167C>T (p.Thr56Met)	CD300E, LOC101928343 (T56M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3140517	NM_181449.3(CD300E):c.115G>A (p.Glu39Lys)	CD300E, LOC101928343 (E39K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2589880	NM_181449.3(CD300E):c.148T>C (p.Cys50Arg)	CD300E, LOC101928343 (C50R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560067	NM_181449.3(CD300E):c.48G>C (p.Leu16Phe)	CD300E, LOC101928343 (L16F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518907	NM_181449.3(CD300E):c.450C>A (p.Asn150Lys)	CD300E, LOC101928343 (N150K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462629	NM_181449.3(CD300E):c.83C>T (p.Ala28Val)	LOC101928343, CD300E (A28V)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2407261	NM_181449.3(CD300E):c.503G>A (p.Arg168Gln)	CD300E, LOC101928343 (R168Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2351332	NM_181449.3(CD300E):c.478G>A (p.Val160Met)	CD300E, LOC101928343 (V160M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2285855	NM_181449.3(CD300E):c.152G>T (p.Arg51Leu)	CD300E, LOC101928343 (R51L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2242408	NM_181449.3(CD300E):c.379G>A (p.Val127Ile)	CD300E, LOC101928343 (V127I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 160836	GRCh38/hg38 17q25.1(chr17:73851698-74610813)x3	BTBD17, CD300A +41 more	Copy number gain	See cases	GBenign
Select item 155275	GRCh38/hg38 17q24.3-25.3(chr17:69916435-83102552)x3	AANAT, AATK +1013 more	Copy number gain	See cases	GPathogenic
Select item 152569	GRCh38/hg38 17q25.1(chr17:73851698-74651858)x3	BTBD17, CD300A +42 more	Copy number gain	See cases	GBenign/Likely benign
Select item 150454	GRCh38/hg38 17q25.1(chr17:73967269-74610906)x3	BTBD17, CD300A +39 more	Copy number gain	See cases	GLikely benign
Select item 148363	GRCh38/hg38 17q23.1-25.1(chr17:36449220-75053130)x3	AARSD1, AATF +2032 more	Copy number gain	See cases	GPathogenic
Select item 145427	GRCh38/hg38 17q25.1(chr17:73851718-74610906)x3	BTBD17, CD300A +41 more	Copy number gain	See cases	GBenign
Select item 59733	GRCh38/hg38 17q25.1(chr17:73851698-74732123)x3	BTBD17, CD300A +44 more	Copy number gain	See cases	GBenign
Select item 59732	GRCh38/hg38 17q25.1(chr17:73843095-74670538)x3	BTBD17, CD300A +42 more	Copy number gain	See cases	GBenign
Select item 58703	GRCh38/hg38 17q24.3-25.3(chr17:69209079-83086677)x3	MIR636, MIR6516 +1033 more	Copy number gain	See cases	GPathogenic
Select item 32717	GRCh38/hg38 17q25.1(chr17:73851698-74610813)x3	BTBD17, CD300A +41 more	Copy number gain	See cases	GConflicting classifications of pathogenicity

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Links from Gene

Items: 21