List of variants in gene LRSAM1 reported as uncertain significance 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: 33

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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.21_41dup (p.Pro10_Lys16dup)	rs760944483	0.00035
NM_001005373.4(LRSAM1):c.1780C>T (p.Arg594Cys)	rs150062009	0.00021
NM_001005373.4(LRSAM1):c.1601C>T (p.Thr534Met)	rs141542114	0.00015
NM_001005373.4(LRSAM1):c.620-3C>T	rs373015900	0.00010
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.1498C>T (p.Leu500Phe)	rs749192098	0.00003
NM_001005373.4(LRSAM1):c.1939G>A (p.Val647Ile)	rs879254326	0.00003
NM_001005373.4(LRSAM1):c.904-4del	rs757987823	0.00002
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.261T>G (p.Asp87Glu)	rs746714138	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.1504-2A>G	rs1064797013
NM_001005373.4(LRSAM1):c.1807A>G (p.Met603Val)
NM_001005373.4(LRSAM1):c.253G>A (p.Val85Ile)	rs765537196
NM_001005373.4(LRSAM1):c.369T>G (p.Ile123Met)
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.917T>C (p.Leu306Pro)	rs140151379

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