List of variants in gene combination KLLN, PTEN reported as uncertain significance for Hereditary cancer-predisposing syndrome

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 66

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HGVS	dbSNP	gnomAD frequency
NM_001126049.2(KLLN):c.-792C>T	rs587779982	0.00044
NM_001126049.2(KLLN):c.-840G>A	rs563841270	0.00036
NM_001126049.2(KLLN):c.-806A>C	rs587782761	0.00004
NM_001126049.2(KLLN):c.-803T>A	rs587782616	0.00003
NM_001126049.2(KLLN):c.-845C>T	rs587782068	0.00003
NM_001126049.2(KLLN):c.-810C>T	rs587781548	0.00001
NM_001126049.2(KLLN):c.-830G>A	rs939612222	0.00001
NM_001126049.2(KLLN):c.-885C>T	rs1042825840	0.00001
NM_001126049.2(KLLN):c.-695G>A	rs587782034
NM_001126049.2(KLLN):c.-695G>C	rs587782034
NM_001126049.2(KLLN):c.-695dup	rs1589593475
NM_001126049.2(KLLN):c.-696G>A
NM_001126049.2(KLLN):c.-697G>A	rs1589593479
NM_001126049.2(KLLN):c.-698G>A	rs1589593482
NM_001126049.2(KLLN):c.-701dup
NM_001126049.2(KLLN):c.-703G>C
NM_001126049.2(KLLN):c.-707T>C	rs1554889795
NM_001126049.2(KLLN):c.-721G>A	rs1589593515
NM_001126049.2(KLLN):c.-726C>T	rs587781465
NM_001126049.2(KLLN):c.-733dup	rs786204897
NM_001126049.2(KLLN):c.-738del	rs1589593532
NM_001126049.2(KLLN):c.-739C>T	rs727502790
NM_001126049.2(KLLN):c.-745C>A	rs1354425960
NM_001126049.2(KLLN):c.-745C>T	rs1354425960
NM_001126049.2(KLLN):c.-747G>A
NM_001126049.2(KLLN):c.-747G>C
NM_001126049.2(KLLN):c.-751C>T
NM_001126049.2(KLLN):c.-766G>A	rs786203383
NM_001126049.2(KLLN):c.-768A>C	rs587782881
NM_001126049.2(KLLN):c.-771G>A
NM_001126049.2(KLLN):c.-785T>C
NM_001126049.2(KLLN):c.-790G>A	rs1232280343
NM_001126049.2(KLLN):c.-797TGC[1]	rs587782867
NM_001126049.2(KLLN):c.-810C>A
NM_001126049.2(KLLN):c.-810C>G	rs587781548
NM_001126049.2(KLLN):c.-812G>A	rs587779981
NM_001126049.2(KLLN):c.-812G>T	rs587779981
NM_001126049.2(KLLN):c.-814C>G	rs1589593635
NM_001126049.2(KLLN):c.-814C>T
NM_001126049.2(KLLN):c.-817C>T	rs1589593642
NM_001126049.2(KLLN):c.-817_-801del	rs1589593611
NM_001126049.2(KLLN):c.-821C>T
NM_001126049.2(KLLN):c.-822C>G
NM_001126049.2(KLLN):c.-822_-821delinsTT	rs1589593646
NM_001126049.2(KLLN):c.-828C>A
NM_001126049.2(KLLN):c.-828C>T	rs786203674
NM_001126049.2(KLLN):c.-830G>C
NM_001126049.2(KLLN):c.-831G>C	rs1589593668
NM_001126049.2(KLLN):c.-831G>T	rs1589593668
NM_001126049.2(KLLN):c.-837T>C	rs112758888
NM_001126049.2(KLLN):c.-837T>G	rs112758888
NM_001126049.2(KLLN):c.-840G>T	rs563841270
NM_001126049.2(KLLN):c.-841G>A	rs1589593700
NM_001126049.2(KLLN):c.-841_-840del	rs786203981
NM_001126049.2(KLLN):c.-845C>G
NM_001126049.2(KLLN):c.-848_-847insA	rs786204886
NM_001126049.2(KLLN):c.-849C>T	rs587782801
NM_001126049.2(KLLN):c.-857C>A
NM_001126049.2(KLLN):c.-857C>G
NM_001126049.2(KLLN):c.-857C>T
NM_001126049.2(KLLN):c.-857del
NM_001126049.2(KLLN):c.-858C>T
NM_001126049.2(KLLN):c.-874G>A	rs1455446453
NM_001126049.2(KLLN):c.-879C>T	rs866859626
NM_001126049.2(KLLN):c.-884C>T	rs1064793239
NM_001126049.2(KLLN):c.-886C>A	rs786204919

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