List of variants in gene TCOF1 reported as benign by PreventionGenetics, part of Exact Sciences

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: 24

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HGVS	dbSNP	gnomAD frequency
NM_001371623.1(TCOF1):c.4172C>T (p.Ala1391Val)	rs15251	0.21165
NM_001371623.1(TCOF1):c.2660T>C (p.Val887Ala)	rs7713638	0.18279
NM_001371623.1(TCOF1):c.1842A>G (p.Ser614=)	rs2071239	0.18176
NM_001371623.1(TCOF1):c.1578C>T (p.Pro526=)	rs2071238	0.17747
NM_001371623.1(TCOF1):c.3530C>G (p.Pro1177Arg)	rs1136103	0.15799
NM_001371623.1(TCOF1):c.1761G>T (p.Gly587=)	rs7701163	0.09554
NM_001371623.1(TCOF1):c.3604-3C>T	rs11743855	0.08821
NM_001371623.1(TCOF1):c.2765C>T (p.Ser922Leu)	rs114689020	0.02268
NM_001371623.1(TCOF1):c.4295G>C (p.Gly1432Ala)	rs45491898	0.01804
NM_001371623.1(TCOF1):c.162A>G (p.Gln54=)	rs73270831	0.01015
NM_001371623.1(TCOF1):c.2245C>T (p.Pro749Ser)	rs73270846	0.00993
NM_001371623.1(TCOF1):c.4007A>G (p.Lys1336Arg)	rs55980697	0.00865
NM_001371623.1(TCOF1):c.579G>A (p.Ala193=)	rs142965998	0.00558
NM_001371623.1(TCOF1):c.2762C>T (p.Pro921Leu)	rs150515843	0.00548
NM_001371623.1(TCOF1):c.1281G>A (p.Ala427=)	rs113299143	0.00291
NM_001371623.1(TCOF1):c.295G>A (p.Ala99Thr)	rs112332762	0.00260
NM_001371623.1(TCOF1):c.3712G>A (p.Ala1238Thr)	rs137960641	0.00205
NM_001371623.1(TCOF1):c.2151T>A (p.Ser717=)	rs141764046	0.00135
NM_001371623.1(TCOF1):c.1590G>A (p.Gly530=)	rs145539529	0.00071
NM_001371623.1(TCOF1):c.2188C>T (p.Pro730Ser)	rs150196623	0.00059
NM_001371623.1(TCOF1):c.4099A>C (p.Lys1367Gln)	rs201234047	0.00031
NM_001371623.1(TCOF1):c.1993G>C (p.Ala665Pro)	rs2071240
NM_001371623.1(TCOF1):c.2659-24_2659-20del	rs151182547
NM_001371623.1(TCOF1):c.4293T>C (p.Gly1431=)

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