STK32C[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 59707	GRCh38/hg38 10q24.31-26.3(chr10:100194215-132432797)x3	EDRF1-AS1, EDRF1-DT +1036 more	Copy number gain	See cases	GPathogenic
Select item 148679	GRCh38/hg38 10q24.31-26.3(chr10:100600492-133622588)x3	GSTO1, GSTO2 +1097 more	Copy number gain	See cases	GPathogenic
Select item 144206	GRCh38/hg38 10q25.1-26.3(chr10:108102587-133620674)x3	LOC126861107, LOC128598885 +802 more	Copy number gain	See cases	GPathogenic
Select item 57507	GRCh38/hg38 10q25.2-26.3(chr10:111313099-133620674)x3	ABLIM1, ABRAXAS2 +679 more	Copy number gain	See cases	GPathogenic
Select item 59728	GRCh38/hg38 10q26.11-26.3(chr10:117866565-133554210)x3	ABRAXAS2, ACADSB +514 more	Copy number gain	See cases	GPathogenic
Select item 153718	GRCh38/hg38 10q26.11-26.3(chr10:119707856-133613639)x3	LOC130004884, LOC130004885 +438 more	Copy number gain	See cases	GPathogenic
Select item 57403	GRCh38/hg38 10q26.12-26.3(chr10:120454430-133620674)x1	LOC130004881, LOC130004882 +418 more	Copy number loss	See cases	GPathogenic
Select item 150499	GRCh38/hg38 10q26.12-26.3(chr10:120970558-133622588)x1	LOC130005014, LOC130005015 +409 more	Copy number loss	See cases	GPathogenic
Select item 154374	GRCh38/hg38 10q26.13-26.3(chr10:121588992-133620674)x1	FUOM, GLRX3 +399 more	Copy number loss	See cases	GPathogenic
Select item 154670	GRCh38/hg38 10q26.13-26.3(chr10:121918547-133620674)x1	LOC130004911, LOC130004912 +395 more	Copy number loss	See cases	GPathogenic
Select item 57376	GRCh38/hg38 10q26.13-26.3(chr10:122265252-133620674)x1	ABRAXAS2, ACADSB +383 more	Copy number loss	See cases	GPathogenic
Select item 149417	GRCh38/hg38 10q26.13-26.3(chr10:122881207-133620609)x1	LOC130004994, LOC130004995 +361 more	Copy number loss	See cases	GPathogenic
Select item 57447	GRCh38/hg38 10q26.13-26.3(chr10:123307835-133620674)x1	ABRAXAS2, ADAM12 +331 more	Copy number loss	See cases	GPathogenic
Select item 155477	GRCh38/hg38 10q26.13-26.3(chr10:123576393-133613639)x1	ABRAXAS2, ADAM12 +318 more	Copy number loss	See cases	GPathogenic
Select item 58822	GRCh38/hg38 10q26.13-26.3(chr10:123580320-133558988)x1	ABRAXAS2, ADAM12 +318 more	Copy number loss	See cases	GPathogenic
Select item 155556	GRCh38/hg38 10q26.13-26.3(chr10:123986772-133613639)x1	ABRAXAS2, ADAM12 +311 more	Copy number loss	See cases	GPathogenic
Select item 146789	GRCh38/hg38 10q26.13-26.3(chr10:124473108-133620609)x1	ABRAXAS2, ADAM12 +297 more	Copy number loss	See cases	GPathogenic
Select item 148580	GRCh38/hg38 10q26.13-26.3(chr10:124834858-133622588)x1	LOC130005026, LOC130005027 +257 more	Copy number loss	See cases	GPathogenic
Select item 150776	GRCh38/hg38 10q26.13-26.3(chr10:125021995-133620609)x1	LOC126861090, LOC126861091 +250 more	Copy number loss	See cases	GPathogenic
Select item 152830	GRCh38/hg38 10q26.13-26.3(chr10:125452905-133785874)x3	ADAM12, ADAM8 +241 more	Copy number gain	See cases	GPathogenic
Select item 144259	GRCh38/hg38 10q26.13-26.3(chr10:125657472-133620674)x1	ADAM12, ADAM8 +234 more	Copy number loss	See cases	GPathogenic
Select item 3061841	GRCh38/hg38 10q26.2-26.3(chr10:125976998-133427130)x1	LOC126861083, LOC126861084 +201 more	Copy number loss	Duane syndrome type 1 +1 more	GPathogenic
Select item 58823	GRCh38/hg38 10q26.2-26.3(chr10:126256585-133613938)x1	ADAM12, ADAM8 +207 more	Copy number loss	See cases	GPathogenic
Select item 144558	GRCh38/hg38 10q26.2-26.3(chr10:126730896-133620609)x1	LOC130005011, LOC130005012 +199 more	Copy number loss	See cases	GPathogenic
Select item 155548	GRCh38/hg38 10q26.2-26.3(chr10:126794646-133613639)x1	ADAM8, ADGRA1 +199 more	Copy number loss	See cases	GPathogenic
Select item 155174	GRCh38/hg38 10q26.2-26.3(chr10:127435985-133622588)x1	ADAM8, ADGRA1 +192 more	Copy number loss	See cases	GPathogenic
Select item 146431	GRCh38/hg38 10q26.2-26.3(chr10:127640489-132776585)x1	AS-PTPRE, BNIP3 +121 more	Copy number loss	See cases	GPathogenic
Select item 152433	GRCh38/hg38 10q26.2-26.3(chr10:127664168-133622588)x3	ADAM8, ADGRA1 +190 more	Copy number gain	See cases	GLikely pathogenic
Select item 149102	GRCh38/hg38 10q26.2-26.3(chr10:127849717-133622588)x1	ADAM8, ADGRA1 +189 more	Copy number loss	See cases	GPathogenic
Select item 149101	GRCh38/hg38 10q26.2-26.3(chr10:128549913-133622588)x1	LOC130004973, LOC130004974 +170 more	Copy number loss	See cases	GPathogenic
Select item 147736	GRCh38/hg38 10q26.3(chr10:128872419-133564028)x3	ADAM8, ADGRA1 +168 more	Copy number gain	See cases	GPathogenic
Select item 148897	GRCh38/hg38 10q26.3(chr10:129427520-133622588)x1	ADAM8, ADGRA1 +165 more	Copy number loss	See cases	GPathogenic
Select item 146234	GRCh38/hg38 10q26.3(chr10:129549258-133620674)x1	LOC130004974, LOC130004975 +163 more	Copy number loss	See cases	GPathogenic
Select item 58825	GRCh38/hg38 10q26.3(chr10:129673966-133613938)x1	ADAM8, ADGRA1 +158 more	Copy number loss	See cases	GPathogenic
Select item 155487	GRCh38/hg38 10q26.3(chr10:130625650-133613639)x1	ADAM8, ADGRA1 +135 more	Copy number loss	See cases	GUncertain significance
Select item 155695	GRCh38/hg38 10q26.3(chr10:131424682-133613639)x1	ADAM8, ADGRA1 +127 more	Copy number loss	See cases	GLikely pathogenic
Select item 57314	GRCh38/hg38 10q26.3(chr10:131457361-133620674)x1	ADAM8, ADGRA1 +127 more	Copy number loss	See cases	GPathogenic
Select item 58853	GRCh38/hg38 10q26.3(chr10:131914873-133613938)x1	ADAM8, ADGRA1 +115 more	Copy number loss	See cases	GPathogenic
Select item 146073	GRCh38/hg38 10q26.3(chr10:132178475-133620674)x1	ADAM8, ADGRA1 +105 more	Copy number loss	See cases	GPathogenic
Select item 716418	NM_173575.4(STK32C):c.1455C>T (p.Ser485=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2520458	NM_173575.4(STK32C):c.1430G>T (p.Gly477Val)	STK32C (G490V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171366	NM_173575.4(STK32C):c.1421C>T (p.Pro474Leu)	STK32C (P474L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323315	NM_173575.4(STK32C):c.1411T>C (p.Ser471Pro)	STK32C (S354P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2366721	NM_173575.4(STK32C):c.1409G>A (p.Arg470His)	STK32C (R353H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3323312	NM_173575.4(STK32C):c.1408C>T (p.Arg470Cys)	STK32C (R353C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 783587	NM_173575.4(STK32C):c.1400A>G (p.Glu467Gly)	STK32C (E350G +2 more)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 3171365	NM_173575.4(STK32C):c.1388C>A (p.Pro463His)	STK32C (P476H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171364	NM_173575.4(STK32C):c.1385A>G (p.Glu462Gly)	STK32C (E462G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171363	NM_173575.4(STK32C):c.1346G>A (p.Arg449Lys)	STK32C (R332K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 708796	NM_173575.4(STK32C):c.1341C>G (p.Leu447=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2459655	NM_173575.4(STK32C):c.1339C>T (p.Leu447Phe)	STK32C (L460F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2295529	NM_173575.4(STK32C):c.1126C>G (p.Arg376Gly)	STK32C (R376G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491160	NM_173575.4(STK32C):c.1105G>A (p.Gly369Ser)	STK32C (G382S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2291151	NM_173575.4(STK32C):c.1094G>T (p.Arg365Met)	STK32C (R248M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225179	NM_173575.4(STK32C):c.1085G>C (p.Ser362Thr)	STK32C (S245T +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3171362	NM_173575.4(STK32C):c.1070T>C (p.Leu357Pro)	STK32C (L240P +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2546069	NM_173575.4(STK32C):c.943G>A (p.Val315Ile)	STK32C (V328I +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323313	NM_173575.4(STK32C):c.937G>A (p.Val313Met)	STK32C (V196M +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2553191	NM_173575.4(STK32C):c.637A>C (p.Ile213Leu)	STK32C (I226L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 768402	NM_173575.4(STK32C):c.624C>T (p.Arg208=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 3171367	NM_173575.4(STK32C):c.574A>T (p.Thr192Ser)	STK32C (T205S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 790633	NM_173575.4(STK32C):c.519A>C (p.Leu173=)	STK32C	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 2257229	NM_173575.4(STK32C):c.452T>A (p.Val151Asp)	STK32C (V34D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3064185	NM_173575.4(STK32C):c.451G>C (p.Val151Leu)	STK32C (V151L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2460708	NM_173575.4(STK32C):c.400G>A (p.Glu134Lys)	STK32C (E147K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2484505	NM_173575.4(STK32C):c.388A>G (p.Ile130Val)	STK32C (I13V +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2493046	NM_173575.4(STK32C):c.338G>A (p.Arg113Gln)	STK32C (R113Q +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 3323316	NM_173575.4(STK32C):c.280C>G (p.Gln94Glu)	STK32C (Q94E +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2256192	NM_173575.4(STK32C):c.128C>T (p.Pro43Leu)	STK32C (P43L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2609124	NM_173575.4(STK32C):c.112C>G (p.Pro38Ala)	STK32C (P38A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2313131	NM_173575.4(STK32C):c.80C>G (p.Ala27Gly)	STK32C (A27G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3323314	NM_173575.4(STK32C):c.70G>A (p.Ala24Thr)	STK32C (A24T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 712971	NM_001318878.2(STK32C):c.196A>G (p.Asn66Asp)	LRRC27, STK32C (N66D)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 3148924	GRCh37/hg19 10q26.12-26.3(chr10:122331280-135426386)x1	ABRAXAS2, ACADSB +80 more	Copy number loss	not provided	GPathogenic
Select item 3063175	GRCh37/hg19 10q26.13-26.3(chr10:125987494-135427143)x1	ABRAXAS2, ADAM12 +55 more	Copy number loss	not specified	GPathogenic
Select item 3063164	GRCh37/hg19 10q23.33-26.3(chr10:95078198-135427143)x3	ABCC2, ABLIM1 +293 more	Copy number gain	not specified	GPathogenic
Select item 3063154	GRCh37/hg19 10q26.3(chr10:131398569-135427143)x1	ADAM8, ADGRA1 +31 more	Copy number loss	not specified	GPathogenic
Select item 3063149	GRCh37/hg19 10q26.13-26.3(chr10:126127397-135427143)x1	ABRAXAS2, ADAM12 +54 more	Copy number loss	not specified	GPathogenic
Select item 3024574	GRCh37/hg19 10q26.3(chr10:131299771-135441274)x1	ADAM8, ADGRA1 +32 more	Copy number loss	not provided	GPathogenic
Select item 2685393	GRCh37/hg19 10q26.3(chr10:133435524-135427143)x1	ADAM8, ADGRA1 +26 more	Copy number loss	not provided	GUncertain significance
Select item 2685391	GRCh37/hg19 10q26.2-26.3(chr10:128925940-135427143)x1	ADAM8, ADGRA1 +38 more	Copy number loss	not provided	GPathogenic
Select item 2684628	GRCh37/hg19 10q26.3(chr10:132852693-134505024)x3	BNIP3, DPYSL4 +9 more	Copy number gain	not provided	GUncertain significance
Select item 2671974	GRCh37/hg19 10q25.1-26.3(chr10:111378692-135427143)x3	ABLIM1, ABRAXAS2 +145 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2671973	GRCh37/hg19 10q26.2-26.3(chr10:128289206-135427143)x1	TCERG1L, TCERG1L-AS1 +38 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2580338	GRCh37/hg19 10q26.13-26.3(chr10:124895517-135440296)x1	ABRAXAS2, ADAM12 +62 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2574696	GRCh37/hg19 10p14-q26.3(chr10:11138692-135427143)	AGAP5, CRTAC1 +682 more	Copy number gain	Distal trisomy 10q	GPathogenic
Select item 2574693	GRCh37/hg19 10q26.13-26.3(chr10:123477898-135427143)	GLRX3, GPR26 +77 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2574686	GRCh37/hg19 10p13-q26.3(chr10:12829206-135427143)	ABRAXAS2, CHCHD1 +673 more	Copy number loss	Distal 10q deletion syndrome	GPathogenic
Select item 2498475	GRCh37/hg19 10q26.12-26.3(chr10:122610933-135439810)x1	ABRAXAS2, ACADSB +80 more	Copy number loss	not provided	GPathogenic
Select item 1809436	GRCh37/hg19 10q26.3(chr10:132631529-135354972)x1	ADAM8, ADGRA1 +27 more	Copy number loss	not provided	GUncertain significance
Select item 1808640	GRCh37/hg19 10q26.2-26.3(chr10:130043370-135345340)x1	ADAM8, ADGRA1 +30 more	Copy number loss	not provided	GPathogenic
Select item 1711099	GRCh37/hg19 10q26.13-26.3(chr10:127198625-135427143)x3	ADAM12, ADAM8 +47 more	Copy number gain	See cases	GPathogenic
Select item 1711096	GRCh37/hg19 10q26.13-26.3(chr10:126914469-135427143)x1	ADAM12, ADAM8 +47 more	Copy number loss	See cases	GPathogenic
Select item 1706486	GRCh37/hg19 10q26.2-26.3(chr10:129605105-135427143)x1	GLRX3, INPP5A +34 more	Copy number loss	See cases	GPathogenic
Select item 1527622	GRCh37/hg19 10q26.2-26.3(chr10:129914228-135427143)	ADAM8, ADGRA1 +32 more	Copy number loss	not specified	GPathogenic
Select item 1527616	GRCh37/hg19 10q26.2-26.3(chr10:128465436-135427143)	ADAM8, ADGRA1 +38 more	Copy number loss	not specified	GPathogenic
Select item 1527609	GRCh37/hg19 10q26.12-26.3(chr10:122343861-135427143)	FAM24A, FAM24B +80 more	Copy number loss	not specified	GPathogenic
Select item 1527608	GRCh37/hg19 10q26.12-26.3(chr10:122125760-135062972)	ABRAXAS2, ACADSB +68 more	Copy number gain	not specified	GLikely pathogenic
Select item 1527605	GRCh37/hg19 10q25.1-26.3(chr10:108455687-135427143)	ABLIM1, ABRAXAS2 +146 more	Copy number gain	not specified	GPathogenic
Select item 1180521	GRCh37/hg19 10q25.3-26.3(chr10:118247181-135435319)x3	ECHS1, EDRF1 +110 more	Copy number gain	not provided	GPathogenic

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