List of variants in gene PLOD1 reported as likely benign for not specified

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: 35

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HGVS	dbSNP	gnomAD frequency
NM_000302.4(PLOD1):c.295G>A (p.Ala99Thr)	rs7551175	0.26545
NM_000302.4(PLOD1):c.358G>T (p.Ala120Ser)	rs2273285	0.14145
NM_000302.4(PLOD1):c.250G>A (p.Ala84Thr)	rs34878020	0.02621
NM_000302.4(PLOD1):c.302+15G>A	rs140227667	0.00760
NM_000302.4(PLOD1):c.1141G>A (p.Val381Met)	rs2230896	0.00668
NM_000302.4(PLOD1):c.975+13C>T	rs79345327	0.00627
NM_000302.4(PLOD1):c.76+17C>T	rs113691754	0.00498
NM_000302.4(PLOD1):c.1534C>T (p.Arg512Cys)	rs138490756	0.00328
NM_000302.4(PLOD1):c.1902+13G>A	rs199765551	0.00259
NM_000302.4(PLOD1):c.1164C>T (p.Thr388=)	rs74949176	0.00170
NM_000302.4(PLOD1):c.843+17G>C	rs201244598	0.00086
NM_000302.4(PLOD1):c.579+17G>A	rs181015965	0.00043
NM_000302.4(PLOD1):c.1707G>A (p.Leu569=)	rs139468110	0.00034
NM_000302.4(PLOD1):c.1428G>A (p.Lys476=)	rs139869965	0.00033
NM_000302.4(PLOD1):c.1495C>T (p.Arg499Trp)	rs149124387	0.00030
NM_000302.4(PLOD1):c.897G>A (p.Pro299=)	rs199946373	0.00015
NM_000302.4(PLOD1):c.303C>T (p.Ser101=)	rs147980436	0.00013
NM_000302.4(PLOD1):c.853C>T (p.Leu285=)	rs370663808	0.00013
NM_000302.4(PLOD1):c.1218G>A (p.Pro406=)	rs754812888	0.00007
NM_000302.4(PLOD1):c.936C>T (p.His312=)	rs374787907	0.00006
NM_000302.4(PLOD1):c.1470+14G>A	rs761691961	0.00005
NM_000302.4(PLOD1):c.-28del	rs1204442973	0.00003
NM_000302.4(PLOD1):c.882C>T (p.Ile294=)	rs747668784	0.00002
NM_000302.4(PLOD1):c.1149T>C (p.Ala383=)	rs1051856481	0.00001
NM_000302.4(PLOD1):c.1461C>T (p.Ile487=)	rs746099980	0.00001
NM_000302.4(PLOD1):c.741+7G>A	rs751215041	0.00001
NM_000302.4(PLOD1):c.-27C>A	rs1252431057
NM_000302.4(PLOD1):c.1098-4G>A	rs1553135998
NM_000302.4(PLOD1):c.1128C>T (p.Thr376=)	rs1553136011
NM_000302.4(PLOD1):c.1471-9_1471-8delinsGT	rs1553136318
NM_000302.4(PLOD1):c.1560C>T (p.Leu520=)
NM_000302.4(PLOD1):c.1903-18C>T	rs750758605
NM_000302.4(PLOD1):c.2028+11G>C	rs1057523876
NM_000302.4(PLOD1):c.210G>A (p.Thr70=)
NM_000302.4(PLOD1):c.77-20A>C

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