List of variants in gene GPD1L reported as likely benign for Brugada syndrome 1

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: 106

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HGVS	dbSNP	gnomAD frequency
NM_015141.4(GPD1L):c.659G>A (p.Arg220His)	rs72546648	0.00130
NM_015141.4(GPD1L):c.459C>T (p.Asn153=)	rs375532052	0.00019
NM_015141.4(GPD1L):c.1038C>T (p.Ser346=)	rs147092668	0.00016
NM_015141.4(GPD1L):c.445C>T (p.Leu149=)	rs146738300	0.00015
NM_015141.4(GPD1L):c.837C>T (p.Phe279=)	rs376724853	0.00013
NM_015141.4(GPD1L):c.192A>G (p.Lys64=)	rs72546651	0.00011
NM_015141.4(GPD1L):c.959+11C>T	rs370985609	0.00011
NM_015141.4(GPD1L):c.876G>A (p.Glu292=)	rs72546642	0.00010
NM_015141.4(GPD1L):c.555T>A (p.Thr185=)	rs151196281	0.00009
NM_015141.4(GPD1L):c.897C>T (p.Leu299=)	rs192905901	0.00009
NM_015141.4(GPD1L):c.906G>A (p.Pro302=)	rs200045526	0.00009
NM_015141.4(GPD1L):c.951A>G (p.Leu317=)	rs746611202	0.00008
NM_015141.4(GPD1L):c.651C>T (p.Asp217=)	rs149641866	0.00006
NM_015141.4(GPD1L):c.996C>T (p.Tyr332=)	rs149423659	0.00006
NM_015141.4(GPD1L):c.246C>T (p.Ser82=)	rs377378878	0.00004
NM_015141.4(GPD1L):c.525C>T (p.Asn175=)	rs142198171	0.00003
NM_015141.4(GPD1L):c.132A>G (p.Glu44=)	rs200273033	0.00002
NM_015141.4(GPD1L):c.54A>G (p.Ser18=)	rs147773109	0.00002
NM_015141.4(GPD1L):c.691C>T (p.Arg231Cys)	rs143486835	0.00002
NM_015141.4(GPD1L):c.759C>G (p.Thr253=)	rs753265220	0.00002
NM_015141.4(GPD1L):c.774C>T (p.Cys258=)	rs753955088	0.00002
NM_015141.4(GPD1L):c.141G>A (p.Val47=)	rs769668097	0.00001
NM_015141.4(GPD1L):c.264A>C (p.Ala88=)	rs528792876	0.00001
NM_015141.4(GPD1L):c.291C>T (p.His97=)	rs1007252272	0.00001
NM_015141.4(GPD1L):c.384C>T (p.Pro128=)	rs779990114	0.00001
NM_015141.4(GPD1L):c.435C>T (p.Asp145=)	rs1367336326	0.00001
NM_015141.4(GPD1L):c.48-4G>T	rs759219954	0.00001
NM_015141.4(GPD1L):c.619-12T>C	rs760328411	0.00001
NM_015141.4(GPD1L):c.630T>C (p.Ala210=)	rs373325536	0.00001
NM_015141.4(GPD1L):c.684C>T (p.Ala228=)	rs545047908	0.00001
NM_015141.4(GPD1L):c.726G>A (p.Arg242=)	rs72546649	0.00001
NM_015141.4(GPD1L):c.729C>A (p.Ile243=)	rs762306432	0.00001
NM_015141.4(GPD1L):c.810G>A (p.Gly270=)	rs945877751	0.00001
NM_015141.4(GPD1L):c.822G>A (p.Arg274=)	rs759180118	0.00001
NM_015141.4(GPD1L):c.846T>A (p.Thr282=)	rs376308565	0.00001
NM_015141.4(GPD1L):c.960-18A>T	rs780858620	0.00001
NM_015141.4(GPD1L):c.1008A>G (p.Pro336=)
NM_015141.4(GPD1L):c.1035G>T (p.Gln345His)	rs780760018
NM_015141.4(GPD1L):c.1050T>C (p.His350=)
NM_015141.4(GPD1L):c.1053A>G (p.Thr351=)
NM_015141.4(GPD1L):c.126C>G (p.Val42=)	rs2125478663
NM_015141.4(GPD1L):c.177C>T (p.Asp59=)
NM_015141.4(GPD1L):c.180T>C (p.His60=)	rs2125478719
NM_015141.4(GPD1L):c.189A>G (p.Val63=)
NM_015141.4(GPD1L):c.195T>C (p.Tyr65=)	rs1700540170
NM_015141.4(GPD1L):c.216A>T (p.Pro72=)
NM_015141.4(GPD1L):c.225+13G>A
NM_015141.4(GPD1L):c.225+14del
NM_015141.4(GPD1L):c.225+20T>A
NM_015141.4(GPD1L):c.226-4G>T
NM_015141.4(GPD1L):c.226-7G>T
NM_015141.4(GPD1L):c.249G>A (p.Glu83=)
NM_015141.4(GPD1L):c.270G>A (p.Leu90=)	rs2125485191
NM_015141.4(GPD1L):c.288C>G (p.Pro96=)
NM_015141.4(GPD1L):c.333G>A (p.Val111=)
NM_015141.4(GPD1L):c.345G>A (p.Ala115=)	rs149167213
NM_015141.4(GPD1L):c.345G>T (p.Ala115=)	rs149167213
NM_015141.4(GPD1L):c.366+13C>A
NM_015141.4(GPD1L):c.366+14A>G
NM_015141.4(GPD1L):c.366+7C>T
NM_015141.4(GPD1L):c.366+9_366+25del	rs776329795
NM_015141.4(GPD1L):c.367-11_367-10delinsAT	rs1575115586
NM_015141.4(GPD1L):c.367-4G>A	rs1700721746
NM_015141.4(GPD1L):c.367-5T>C	rs2125486240
NM_015141.4(GPD1L):c.372A>C (p.Ile124=)
NM_015141.4(GPD1L):c.47+19G>C
NM_015141.4(GPD1L):c.48-13A>G
NM_015141.4(GPD1L):c.48-15C>T
NM_015141.4(GPD1L):c.480A>C (p.Ala160=)
NM_015141.4(GPD1L):c.483G>A (p.Glu161=)
NM_015141.4(GPD1L):c.505+8C>G
NM_015141.4(GPD1L):c.506-19T>C
NM_015141.4(GPD1L):c.506-9T>C
NM_015141.4(GPD1L):c.510C>T (p.Ser170=)
NM_015141.4(GPD1L):c.570T>C (p.Ile190=)
NM_015141.4(GPD1L):c.573C>T (p.Thr191=)
NM_015141.4(GPD1L):c.594T>C (p.Thr198=)
NM_015141.4(GPD1L):c.612G>A (p.Ala204=)
NM_015141.4(GPD1L):c.612G>T (p.Ala204=)	rs770011428
NM_015141.4(GPD1L):c.618+15_618+16del
NM_015141.4(GPD1L):c.618+8C>T
NM_015141.4(GPD1L):c.619-9C>A	rs2044880
NM_015141.4(GPD1L):c.648C>T (p.Cys216=)
NM_015141.4(GPD1L):c.675C>G (p.Thr225=)
NM_015141.4(GPD1L):c.681G>A (p.Ala227=)	rs973664942
NM_015141.4(GPD1L):c.696G>A (p.Leu232=)
NM_015141.4(GPD1L):c.69A>C (p.Ile23=)
NM_015141.4(GPD1L):c.762C>T (p.Phe254=)	rs1453406813
NM_015141.4(GPD1L):c.798C>T (p.Thr266=)
NM_015141.4(GPD1L):c.813G>A (p.Arg271=)	rs35464343
NM_015141.4(GPD1L):c.820A>C (p.Arg274=)	rs1701039817
NM_015141.4(GPD1L):c.828C>A (p.Ala276=)
NM_015141.4(GPD1L):c.834C>G (p.Ala278=)	rs1204498854
NM_015141.4(GPD1L):c.852+12C>T
NM_015141.4(GPD1L):c.852+14T>G
NM_015141.4(GPD1L):c.853-15T>A
NM_015141.4(GPD1L):c.906G>T (p.Pro302=)	rs200045526
NM_015141.4(GPD1L):c.959+12A>C
NM_015141.4(GPD1L):c.959+15C>T
NM_015141.4(GPD1L):c.959+20A>T
NM_015141.4(GPD1L):c.959+7C>A	rs1057523126
NM_015141.4(GPD1L):c.960-14T>C
NM_015141.4(GPD1L):c.960-4C>T
NM_015141.4(GPD1L):c.960-6A>C
NM_015141.4(GPD1L):c.960-8C>T
NM_015141.4(GPD1L):c.978A>C (p.Ala326=)	rs1553663699

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