List of variants in gene STK11 reported as likely benign by Quest Diagnostics Nichols Institute San Juan Capistrano

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: 31

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HGVS	dbSNP	gnomAD frequency
NM_000455.5(STK11):c.*8C>T	rs587782259	0.00027
NM_000455.5(STK11):c.237C>T (p.Ile79=)	rs751859508	0.00005
NM_000455.5(STK11):c.366G>A (p.Lys122=)	rs376969448	0.00005
NM_000455.5(STK11):c.465-5C>T	rs567202367	0.00005
NM_000455.5(STK11):c.970C>G (p.Pro324Ala)	rs549474196	0.00005
NM_000455.5(STK11):c.374+9T>A	rs762297795	0.00003
NM_000455.5(STK11):c.615G>A (p.Ala205=)	rs532889728	0.00003
NM_000455.5(STK11):c.735C>G (p.Leu245=)	rs773147894	0.00002
NM_000455.5(STK11):c.771G>A (p.Gly257=)	rs777998890	0.00002
NM_000455.5(STK11):c.828C>T (p.Gly276=)	rs200824447	0.00002
NM_000455.5(STK11):c.1109-4C>T	rs1407794756	0.00001
NM_000455.5(STK11):c.1128G>A (p.Glu376=)	rs747018506	0.00001
NM_000455.5(STK11):c.1190C>T (p.Ala397Val)	rs558040549	0.00001
NM_000455.5(STK11):c.180C>T (p.Tyr60=)	rs778376925	0.00001
NM_000455.5(STK11):c.312G>A (p.Arg104=)	rs780749732	0.00001
NM_000455.5(STK11):c.348G>T (p.Val116=)	rs774482643	0.00001
NM_000455.5(STK11):c.621C>T (p.Asp207=)	rs569380138	0.00001
NM_000455.5(STK11):c.648C>T (p.Ser216=)	rs376083300	0.00001
NM_000455.5(STK11):c.720G>A (p.Ser240=)	rs759743897	0.00001
NM_000455.5(STK11):c.801C>T (p.Ile267=)	rs539772540	0.00001
NM_000455.5(STK11):c.846C>G (p.Leu282=)	rs777872290	0.00001
NM_000455.5(STK11):c.863-4T>C	rs778853572	0.00001
NM_000455.5(STK11):c.882G>A (p.Pro294=)	rs587781178	0.00001
NM_000455.5(STK11):c.921-9C>T	rs761688641	0.00001
NM_000455.5(STK11):c.117C>T (p.Arg39=)	rs786203942
NM_000455.5(STK11):c.1191G>A (p.Ala397=)	rs774759899
NM_000455.5(STK11):c.1212C>T (p.Ser404=)	rs754945004
NM_000455.5(STK11):c.537G>A (p.Pro179=)	rs528535500
NM_000455.5(STK11):c.666C>G (p.Pro222=)	rs542189325
NM_000455.5(STK11):c.920+7G>A	rs2075607
NM_000455.5(STK11):c.942T>C (p.Pro314=)	rs1256260277

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