List of variants in gene APC reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 30

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HGVS	dbSNP	gnomAD frequency
NM_000038.6(APC):c.4336G>A (p.Ala1446Thr)	rs146572883	0.00056
NM_000038.6(APC):c.295C>T (p.Arg99Trp)	rs139196838	0.00048
NM_000038.6(APC):c.3352A>G (p.Asn1118Asp)	rs140493115	0.00021
NM_000038.6(APC):c.5009C>T (p.Ala1670Val)	rs202228932	0.00018
NM_000038.6(APC):c.3479C>A (p.Thr1160Lys)	rs201004111	0.00017
NM_000038.6(APC):c.7193C>T (p.Ser2398Phe)	rs150882838	0.00017
NM_000038.6(APC):c.1631T>C (p.Ile544Thr)	rs144056494	0.00012
NM_000038.6(APC):c.95A>G (p.Asn32Ser)	rs539108537	0.00009
NM_000038.6(APC):c.4072G>A (p.Ala1358Thr)	rs139618756	0.00006
NM_000038.6(APC):c.1627-10T>G	rs863224538	0.00003
NM_000038.6(APC):c.8017A>G (p.Arg2673Gly)	rs767286063	0.00002
NM_000038.6(APC):c.8199A>G (p.Gln2733=)	rs372365378	0.00002
NM_000038.6(APC):c.1243G>A (p.Ala415Thr)	rs756336949	0.00001
NM_000038.6(APC):c.268A>G (p.Lys90Glu)	rs763184444	0.00001
NM_000038.6(APC):c.3218C>T (p.Thr1073Ile)	rs773354366	0.00001
NM_000038.6(APC):c.6658A>G (p.Asn2220Asp)	rs374464049	0.00001
NM_000038.6(APC):c.193C>A (p.Gln65Lys)	rs863225320
NM_000038.6(APC):c.2060T>G (p.Leu687Arg)	rs863225324
NM_000038.6(APC):c.244T>A (p.Phe82Ile)	rs863225329
NM_000038.6(APC):c.3077A>C (p.Asn1026Thr)	rs1114167603
NM_000038.6(APC):c.3937A>G (p.Thr1313Ala)	rs863225349
NM_000038.6(APC):c.4222G>A (p.Glu1408Lys)	rs1554085632
NM_000038.6(APC):c.423-3T>A	rs587782293
NM_000038.6(APC):c.423-3_423-2del	rs863225354
NM_000038.6(APC):c.4354G>T (p.Val1452Leu)	rs1172454959
NM_000038.6(APC):c.6565A>C (p.Lys2189Gln)	rs1554087525
NM_000038.6(APC):c.6814A>G (p.Arg2272Gly)	rs1561610453
NM_000038.6(APC):c.7264A>T (p.Thr2422Ser)	rs730881260
NM_000038.6(APC):c.7726G>A (p.Ala2576Thr)	rs1554088617
NM_000038.6(APC):c.934G>A (p.Val312Met)	rs1060503285

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