List of variants in gene LRSAM1 reported as uncertain significance for not provided

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: 61

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HGVS	dbSNP	gnomAD frequency
NM_001005373.4(LRSAM1):c.814C>T (p.Arg272Trp)	rs149456922	0.00063
NM_001005373.4(LRSAM1):c.414G>A (p.Lys138=)	rs151323851	0.00056
NM_001005373.4(LRSAM1):c.586G>A (p.Gly196Ser)	rs148059394	0.00045
NM_001005373.4(LRSAM1):c.917T>G (p.Leu306Arg)	rs140151379	0.00039
NM_001005373.4(LRSAM1):c.2111G>A (p.Arg704His)	rs140808447	0.00035
NM_001005373.4(LRSAM1):c.21_41dup (p.Pro10_Lys16dup)	rs760944483	0.00035
NM_001005373.4(LRSAM1):c.720C>G (p.Asp240Glu)	rs150820300	0.00024
NM_001005373.4(LRSAM1):c.1780C>T (p.Arg594Cys)	rs150062009	0.00021
NM_001005373.4(LRSAM1):c.497C>T (p.Pro166Leu)	rs142085060	0.00019
NM_001005373.4(LRSAM1):c.1601C>T (p.Thr534Met)	rs141542114	0.00015
NM_001005373.4(LRSAM1):c.1088+1G>C	rs765641195	0.00014
NM_001005373.4(LRSAM1):c.2110C>T (p.Arg704Cys)	rs150984897	0.00011
NM_001005373.4(LRSAM1):c.620-3C>T	rs373015900	0.00010
NM_001005373.4(LRSAM1):c.1153G>A (p.Val385Ile)	rs373570877	0.00009
NM_001005373.4(LRSAM1):c.1422+6C>T	rs745690669	0.00006
NM_001005373.4(LRSAM1):c.1949C>T (p.Thr650Met)	rs773505699	0.00006
NM_001005373.4(LRSAM1):c.436G>A (p.Val146Met)	rs555377969	0.00006
NM_001005373.4(LRSAM1):c.1347+5G>A	rs368570954	0.00005
NM_001005373.4(LRSAM1):c.136T>C (p.Phe46Leu)	rs546739304	0.00004
NM_001005373.4(LRSAM1):c.1781G>A (p.Arg594His)	rs537838691	0.00004
NM_001005373.4(LRSAM1):c.1877T>G (p.Val626Gly)	rs574202204	0.00004
NM_001005373.4(LRSAM1):c.2152C>T (p.Arg718Cys)	rs368202093	0.00004
NM_001005373.4(LRSAM1):c.685G>A (p.Glu229Lys)	rs563259179	0.00004
NM_001005373.4(LRSAM1):c.1498C>T (p.Leu500Phe)	rs749192098	0.00003
NM_001005373.4(LRSAM1):c.1939G>A (p.Val647Ile)	rs879254326	0.00003
NM_001005373.4(LRSAM1):c.1714C>T (p.Arg572Cys)	rs1359751742	0.00002
NM_001005373.4(LRSAM1):c.2009T>C (p.Val670Ala)	rs748185533	0.00002
NM_001005373.4(LRSAM1):c.49C>T (p.Arg17Cys)	rs770259167	0.00002
NM_001005373.4(LRSAM1):c.904-4del	rs757987823	0.00002
NM_001005373.4(LRSAM1):c.1094G>A (p.Arg365Lys)	rs1381062773	0.00001
NM_001005373.4(LRSAM1):c.1267G>A (p.Glu423Lys)	rs767351229	0.00001
NM_001005373.4(LRSAM1):c.1348-6T>A	rs200130803	0.00001
NM_001005373.4(LRSAM1):c.1454T>C (p.Leu485Pro)	rs369939320	0.00001
NM_001005373.4(LRSAM1):c.1589G>A (p.Arg530Gln)	rs760321710	0.00001
NM_001005373.4(LRSAM1):c.1619G>T (p.Ser540Ile)	rs1400819662	0.00001
NM_001005373.4(LRSAM1):c.184G>A (p.Val62Ile)	rs570688892	0.00001
NM_001005373.4(LRSAM1):c.1870C>G (p.Arg624Gly)	rs375938990	0.00001
NM_001005373.4(LRSAM1):c.2146C>T (p.Arg716Cys)	rs772786050	0.00001
NM_001005373.4(LRSAM1):c.261T>G (p.Asp87Glu)	rs746714138	0.00001
NM_001005373.4(LRSAM1):c.362G>A (p.Arg121His)	rs143910539	0.00001
NM_001005373.4(LRSAM1):c.972G>A (p.Leu324=)	rs940085400	0.00001
NM_001005373.4(LRSAM1):c.1043+1G>A	rs373571535
NM_001005373.4(LRSAM1):c.121C>G (p.Leu41Val)	rs1834465235
NM_001005373.4(LRSAM1):c.1262T>A (p.Met421Lys)
NM_001005373.4(LRSAM1):c.1430T>C (p.Leu477Ser)	rs1835920830
NM_001005373.4(LRSAM1):c.146T>C (p.Phe49Ser)	rs942509436
NM_001005373.4(LRSAM1):c.1504-2A>G	rs1064797013
NM_001005373.4(LRSAM1):c.1807A>G (p.Met603Val)
NM_001005373.4(LRSAM1):c.1831G>A (p.Val611Met)	rs771783337
NM_001005373.4(LRSAM1):c.1889_1894del (p.Leu630_Ala632delinsPro)	rs1564283769
NM_001005373.4(LRSAM1):c.2108T>C (p.Leu703Pro)	rs1588144691
NM_001005373.4(LRSAM1):c.253G>A (p.Val85Ile)	rs765537196
NM_001005373.4(LRSAM1):c.369T>G (p.Ile123Met)
NM_001005373.4(LRSAM1):c.406+5G>A	rs1834732559
NM_001005373.4(LRSAM1):c.528+5A>G
NM_001005373.4(LRSAM1):c.593C>A (p.Ala198Glu)	rs758867006
NM_001005373.4(LRSAM1):c.595G>A (p.Ala199Thr)	rs745326217
NM_001005373.4(LRSAM1):c.643C>A (p.Pro215Thr)	rs765389102
NM_001005373.4(LRSAM1):c.736G>A (p.Glu246Lys)	rs2132048180
NM_001005373.4(LRSAM1):c.818G>A (p.Arg273His)	rs368088593
NM_001005373.4(LRSAM1):c.917T>C (p.Leu306Pro)	rs140151379

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