List of variants in gene BUB1B reported as uncertain significance for colorectal neoplasm

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 14

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HGVS	dbSNP	gnomAD frequency
NM_001211.6(BUB1B):c.1001C>T (p.Pro334Leu)	rs141953425	0.00063
NM_001211.6(BUB1B):c.805A>G (p.Asn269Asp)	rs148159407	0.00041
NM_001211.6(BUB1B):c.1943C>T (p.Thr648Ile)	rs148348158	0.00016
NM_001211.6(BUB1B):c.1478C>T (p.Thr493Ile)	rs146795655	0.00011
NM_001211.6(BUB1B):c.1630C>T (p.Pro544Ser)	rs138332995	0.00011
NM_001211.6(BUB1B):c.1361A>G (p.Lys454Arg)	rs373256667	0.00004
NM_001211.6(BUB1B):c.1382A>C (p.Gln461Pro)	rs747886467	0.00004
NM_001211.6(BUB1B):c.2530C>T (p.Leu844Phe)	rs28989181	0.00002
NM_001211.6(BUB1B):c.234G>T (p.Trp78Cys)	rs760085736	0.00001
NM_001211.6(BUB1B):c.242A>G (p.Tyr81Cys)	rs1212671249	0.00001
NM_001211.6(BUB1B):c.1168GAG[1] (p.Glu391del)	rs778590557
NM_001211.6(BUB1B):c.1453G>A (p.Glu485Lys)	rs770704003
NM_001211.6(BUB1B):c.458A>T (p.Gln153Leu)	rs776363221
NM_001211.6(BUB1B):c.737G>A (p.Gly246Glu)	rs1407334063

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