List of variants in gene BRAT1 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_152743.4(BRAT1):c.1828C>T (p.Arg610Trp)	rs61753094	0.00152
NM_152743.4(BRAT1):c.434C>T (p.Ala145Val)	rs140833277	0.00095
NM_152743.4(BRAT1):c.1594G>A (p.Gly532Arg)	rs142129866	0.00028
NM_152743.4(BRAT1):c.2009G>A (p.Arg670His)	rs147119058	0.00011
NM_152743.4(BRAT1):c.1340C>T (p.Thr447Met)	rs368808380	0.00008
NM_152743.4(BRAT1):c.920A>C (p.His307Pro)	rs778881636	0.00003
NM_152743.4(BRAT1):c.1522C>T (p.Arg508Cys)	rs751548415	0.00002
NM_152743.4(BRAT1):c.2092G>A (p.Val698Met)	rs781355172	0.00002
NM_152743.4(BRAT1):c.1129C>T (p.Pro377Ser)	rs780327501	0.00001
NM_152743.4(BRAT1):c.1135-4G>A	rs1404214519	0.00001
NM_152743.4(BRAT1):c.1280G>A (p.Arg427Gln)	rs375466838	0.00001
NM_152743.4(BRAT1):c.158C>G (p.Pro53Arg)	rs368397368	0.00001
NM_152743.4(BRAT1):c.853C>T (p.Arg285Trp)	rs1301692811	0.00001
NM_152743.4(BRAT1):c.113C>T (p.Thr38Met)	rs1780250788
NM_152743.4(BRAT1):c.1267G>A (p.Val423Ile)	rs141807337
NM_152743.4(BRAT1):c.2298C>A (p.Asp766Glu)	rs144085416
NM_152743.4(BRAT1):c.983T>C (p.Leu328Pro)	rs1291695271

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