SPINK9[gene] - ClinVar

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Items: 23

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59672	GRCh38/hg38 5q21.3-33.2(chr5:106619588-156124387)x1	ABLIM3, ACSL6 +1672 more	Copy number loss	See cases	GPathogenic
Select item 149858	GRCh38/hg38 5q23.3-33.2(chr5:129847794-153353546)x3	LOC129994992, LOC129994993 +1157 more	Copy number gain	See cases	GPathogenic
Select item 57483	GRCh38/hg38 5q23.3-33.2(chr5:130860928-155321811)x3	ABLIM3, ACSL6 +1218 more	Copy number gain	See cases	GPathogenic
Select item 150685	GRCh38/hg38 5q31.3-32(chr5:141089988-149530678)x3	ABLIM3, ADRB2 +313 more	Copy number gain	See cases	GPathogenic
Select item 147500	GRCh38/hg38 5q32(chr5:145197355-148541511)x1	C5orf46, CTB-99A3.1 +82 more	Copy number loss	See cases	GPathogenic
Select item 3322254	NM_001040433.2(SPINK9):c.14C>G (p.Ala5Gly)	FBXO38-DT, SPINK9 (A5G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3322255	NM_001040433.2(SPINK9):c.18A>G (p.Ile6Met)	FBXO38-DT, SPINK9 (I6M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169160	NM_001040433.2(SPINK9):c.34C>A (p.Leu12Met)	FBXO38-DT, SPINK9 (L12M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2480032	NM_001040433.2(SPINK9):c.38C>T (p.Thr13Ile)	FBXO38-DT, SPINK9 (T13I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169161	NM_001040433.2(SPINK9):c.50T>C (p.Met17Thr)	FBXO38-DT, SPINK9 (M17T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3169162	NM_001040433.2(SPINK9):c.65G>A (p.Cys22Tyr)	FBXO38-DT, SPINK9 (C22Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275367	NM_001040433.2(SPINK9):c.163G>A (p.Gly55Arg)	FBXO38-DT, SPINK9 (G55R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1808574	GRCh37/hg19 5q32(chr5:147164969-149315489)x1	ABLIM3, ADRB2 +23 more	Copy number loss	not provided	GPathogenic
Select item 687529	GRCh37/hg19 5q31.3-32(chr5:140424333-148985999)x3	ABLIM3, ADRB2 +92 more	Copy number gain	not provided	GUncertain significance
Select item 635930	Single allele	C5orf24, C5orf34 +600 more	Deletion	Neurodevelopmental disorder	GUncertain significance
Select item 457359	NC_000005.9:g.(?_86400000)_(154000000_?)del	CCDC69, CCNH +385 more	Deletion	Familial adenomatous polyposis 1 +1 more	GPathogenic
Select item 442532	GRCh37/hg19 5q32(chr5:147713457-147774708)x3	FBXO38, SPINK9	Copy number gain	See cases	GUncertain significance
Select item 442431	GRCh37/hg19 5p15.1-q35.2(chr5:17628741-176575720)x1	DHFR, DHX29 +738 more	Copy number loss	See cases	GPathogenic
Select item 442272	GRCh37/hg19 5q31.3-32(chr5:141113273-149154835)x1	ABLIM3, ADRB2 +48 more	Copy number loss	See cases	GPathogenic
Select item 441920	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 441919	GRCh37/hg19 5p15.33-q35.3(chr5:113577-180719789)x3	ABLIM3, ACOT12 +870 more	Copy number gain	See cases	GPathogenic
Select item 425542	GRCh37/hg19 5q15-35.3(chr5:94844077-178830410)x3	ARL10, ARL14EPL +511 more	Copy number gain	not provided	GLikely benign
Select item 394550	GRCh37/hg19 5q21.3-35.3(chr5:106716357-180687338)x3	HRH2, HSD17B4 +520 more	Copy number gain	See cases	GPathogenic

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Items: 23