List of variants in gene CPT2 reported as uncertain significance by Illumina Laboratory Services, Illumina

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: 38

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HGVS	dbSNP	gnomAD frequency
NM_000098.3(CPT2):c.1806T>C (p.Phe602=)	rs147953465	0.00245
NM_000098.3(CPT2):c.*55C>T	rs61561746	0.00201
NM_000098.3(CPT2):c.1025T>C (p.Met342Thr)	rs144658100	0.00110
NM_000098.3(CPT2):c.321A>G (p.Lys107=)	rs147846614	0.00045
NM_000098.3(CPT2):c.1477G>A (p.Ala493Thr)	rs61731996	0.00038
NM_000098.3(CPT2):c.*361T>C	rs558161718	0.00034
NM_000098.3(CPT2):c.500G>A (p.Arg167Gln)	rs144760921	0.00028
NM_000098.3(CPT2):c.236A>C (p.Lys79Thr)	rs150888506	0.00027
NM_000098.3(CPT2):c.1048C>T (p.Arg350Cys)	rs151003641	0.00025
NM_000098.3(CPT2):c.1438G>A (p.Gly480Arg)	rs201508063	0.00020
NM_000098.3(CPT2):c.*223A>C	rs758780739	0.00017
NM_000098.2(CPT2):c.-282C>T	rs886046402	0.00009
NM_000098.3(CPT2):c.*439T>C	rs886046410	0.00008
NM_000098.3(CPT2):c.1202G>T (p.Ser401Ile)	rs146670074	0.00007
NM_000098.2(CPT2):c.-285C>A	rs577034240	0.00006
NM_000098.3(CPT2):c.1737C>T (p.Tyr579=)	rs957344521	0.00006
NM_000098.3(CPT2):c.1335C>T (p.Cys445=)	rs143075786	0.00005
NM_000098.3(CPT2):c.1645+15G>T	rs753344588	0.00004
NM_000098.2(CPT2):c.-216A>G	rs886046404	0.00003
NM_000098.3(CPT2):c.1559C>T (p.Pro520Leu)	rs776754218	0.00003
NM_000098.3(CPT2):c.852C>T (p.Pro284=)	rs138575554	0.00003
NM_000098.3(CPT2):c.339G>A (p.Ser113=)	rs778017005	0.00002
NM_000098.2(CPT2):c.-229G>T	rs886046403	0.00001
NM_000098.2(CPT2):c.-461T>C	rs17848481	0.00001
NM_000098.3(CPT2):c.*81C>T	rs1035232426	0.00001
NM_000098.3(CPT2):c.1158A>C (p.Glu386Asp)	rs758408111	0.00001
NM_000098.3(CPT2):c.1476C>T (p.Ala492=)	rs548364005	0.00001
NM_000098.3(CPT2):c.1508G>A (p.Arg503His)	rs750079911	0.00001
NM_000098.3(CPT2):c.1897G>T (p.Ala633Ser)	rs141903761	0.00001
NM_000098.2(CPT2):c.-242G>C	rs548768045
NM_000098.3(CPT2):c.*142T>C	rs1256527025
NM_000098.3(CPT2):c.1064C>G (p.Ser355Cys)	rs1645419768
NM_000098.3(CPT2):c.1721A>C (p.Tyr574Ser)	rs1645442128
NM_000098.3(CPT2):c.1936G>A (p.Asp646Asn)	rs369202713
NM_000098.3(CPT2):c.388A>C (p.Asn130His)	rs886046408
NM_000098.3(CPT2):c.411C>G (p.Phe137Leu)	rs1645411725
NM_000098.3(CPT2):c.448A>G (p.Thr150Ala)	rs141505320
NM_000098.3(CPT2):c.683A>G (p.Lys228Arg)	rs886046409

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