List of variants in gene combination HRAS, LRRC56 reported as likely benign by GeneDx

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_005343.4(HRAS):c.451-48C>T	rs45607337	0.01453
NM_005343.4(HRAS):c.451-341G>A	rs45489193	0.00945
NM_005343.4(HRAS):c.*76G>C	rs45565838	0.00511
NM_005343.4(HRAS):c.450+174G>A	rs371117417	0.00008
NM_005343.4(HRAS):c.42G>A (p.Val14=)	rs777038147	0.00006
NM_005343.4(HRAS):c.222C>T (p.Thr74=)	rs372223975	0.00005
NM_005343.4(HRAS):c.508A>T (p.Lys170Ter)	rs372936166	0.00005
NM_005343.4(HRAS):c.-54+7G>A	rs1183370084	0.00004
NM_005343.4(HRAS):c.534C>G (p.Gly178=)	rs770431635	0.00004
NM_005343.4(HRAS):c.291-8C>T	rs1057522962	0.00003
NM_005343.4(HRAS):c.54G>A (p.Ala18=)	rs148380285	0.00003
NM_005343.4(HRAS):c.84T>C (p.Phe28=)	rs915086641	0.00002
NM_005343.4(HRAS):c.*5+14C>G	rs587780953	0.00001
NM_005343.4(HRAS):c.*6-2A>C	rs730880459	0.00001
NM_005343.4(HRAS):c.-19C>T	rs1187467800	0.00001
NM_005343.4(HRAS):c.111+14C>T	rs372917082	0.00001
NM_005343.4(HRAS):c.150G>A (p.Thr50=)	rs1057520421	0.00001
NM_005343.4(HRAS):c.228G>A (p.Glu76=)	rs1057522598	0.00001
NM_005343.4(HRAS):c.24G>C (p.Val8=)	rs1451160542	0.00001
NM_005343.4(HRAS):c.302A>G (p.Lys101Arg)	rs1131691997	0.00001
NM_005343.4(HRAS):c.426C>T (p.Ile142=)	rs533567288	0.00001
NM_005343.4(HRAS):c.450+18C>T	rs1057522255	0.00001
NM_005343.4(HRAS):c.516C>T (p.Asn172=)	rs765180494	0.00001
NM_005343.4(HRAS):c.537C>T (p.Pro179=)	rs371316832	0.00001
NM_005343.4(HRAS):c.64C>T (p.Gln22Ter)	rs121917757	0.00001
NM_176795.5(HRAS):c.480C>T (p.Ser160=)	rs1057522069	0.00001
NM_176795.5(HRAS):c.498C>G (p.Pro166=)	rs377676071	0.00001
NM_176795.5(HRAS):c.501G>A (p.Pro167=)	rs764211685	0.00001
NM_005343.4(HRAS):c.162C>T (p.Asp54=)	rs1057520410
NM_005343.4(HRAS):c.234C>T (p.Phe78=)	rs1057522882
NM_005343.4(HRAS):c.291-17C>G	rs753558541
NM_005343.4(HRAS):c.312G>A (p.Lys104=)	rs1060504682
NM_005343.4(HRAS):c.451-5C>T	rs370181298
NM_005343.4(HRAS):c.96C>T (p.Tyr32=)	rs369039481
NM_176795.5(HRAS):c.500C>T (p.Pro167Leu)	rs730880457

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