List of variants reported as uncertain significance for adenoma by Baylor Genetics

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		ClinVar version:

Total variants: 53

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.7823G>A (p.Arg2608His)	rs202052174	0.00059
NM_003977.4(AIP):c.807C>T (p.Phe269=)	rs139407567	0.00055
NM_003977.4(AIP):c.382C>T (p.Arg128Cys)	rs140530307	0.00054
NM_022124.6(CDH23):c.3022G>A (p.Val1008Met)	rs201053044	0.00043
NM_022124.6(CDH23):c.9569C>T (p.Ala3190Val)	rs111033536	0.00037
NM_022124.6(CDH23):c.9524G>A (p.Arg3175His)	rs140884994	0.00023
NM_022124.6(CDH23):c.4405A>G (p.Ile1469Val)	rs200635365	0.00014
NM_003977.4(AIP):c.733G>A (p.Glu245Lys)	rs150645662	0.00012
NM_003977.4(AIP):c.974G>A (p.Arg325Gln)	rs754619109	0.00011
NM_022124.6(CDH23):c.5228C>A (p.Thr1743Asn)	rs191021194	0.00010
NM_003977.4(AIP):c.827C>T (p.Ala276Val)	rs61741147	0.00009
NM_022124.6(CDH23):c.1282G>A (p.Asp428Asn)	rs188376296	0.00009
NM_003977.4(AIP):c.205A>G (p.Lys69Glu)	rs141223463	0.00008
NM_022124.6(CDH23):c.3397G>A (p.Glu1133Lys)	rs111033509	0.00008
NM_003977.4(AIP):c.572G>A (p.Arg191His)	rs141826817	0.00007
NM_003977.4(AIP):c.355C>T (p.Arg119Trp)	rs368933035	0.00004
NM_003977.4(AIP):c.692C>T (p.Thr231Met)	rs532170807	0.00004
NM_003977.4(AIP):c.70G>C (p.Glu24Gln)	rs267606568	0.00004
NM_022124.6(CDH23):c.9566G>A (p.Arg3189Gln)	rs727502936	0.00004
NM_022124.6(CDH23):c.982G>A (p.Ala328Thr)	rs374545987	0.00004
NM_003977.4(AIP):c.563G>A (p.Arg188Gln)	rs866556486	0.00003
NM_022124.6(CDH23):c.7466G>A (p.Arg2489His)	rs141986620	0.00003
NM_003977.4(AIP):c.415G>T (p.Asp139Tyr)	rs138312605	0.00002
NM_003977.4(AIP):c.727G>T (p.Val243Leu)	rs1385147597	0.00002
NM_003977.4(AIP):c.784G>A (p.Asp262Asn)	rs758918509	0.00002
NM_003977.4(AIP):c.908G>A (p.Ser303Asn)	rs1006697477	0.00002
NM_003977.4(AIP):c.115C>T (p.Arg39Trp)	rs781366620	0.00001
NM_003977.4(AIP):c.140G>A (p.Gly47Asp)	rs1164577485	0.00001
NM_003977.4(AIP):c.160C>T (p.Arg54Trp)	rs752553438	0.00001
NM_003977.4(AIP):c.174G>C (p.Lys58Asn)	rs267606539	0.00001
NM_003977.4(AIP):c.316C>T (p.Arg106Cys)	rs369414668	0.00001
NM_003977.4(AIP):c.419C>T (p.Ala140Val)	rs762219351	0.00001
NM_003977.4(AIP):c.476G>A (p.Ser159Asn)	rs536239840	0.00001
NM_003977.4(AIP):c.571C>T (p.Arg191Cys)	rs189861025	0.00001
NM_003977.4(AIP):c.73C>T (p.Leu25Phe)	rs777083581	0.00001
NM_003977.4(AIP):c.745G>A (p.Glu249Lys)	rs1313811815	0.00001
NM_003977.4(AIP):c.79G>C (p.Asp27His)	rs1024903808	0.00001
NM_003977.4(AIP):c.136G>A (p.Glu46Lys)	rs772580337
NM_003977.4(AIP):c.151G>A (p.Asp51Asn)	rs1591042638
NM_003977.4(AIP):c.164C>T (p.Ala55Val)	rs1865805899
NM_003977.4(AIP):c.16G>A (p.Ala6Thr)
NM_003977.4(AIP):c.261G>C (p.Gln87His)	rs767982777
NM_003977.4(AIP):c.279G>A (p.Lys93=)
NM_003977.4(AIP):c.474G>T (p.Glu158Asp)	rs1245383191
NM_003977.4(AIP):c.485C>T (p.Thr162Met)	rs764344774
NM_003977.4(AIP):c.523A>C (p.Lys175Gln)
NM_003977.4(AIP):c.649C>G (p.Gln217Glu)
NM_003977.4(AIP):c.807C>G (p.Phe269Leu)
NM_003977.4(AIP):c.879G>T (p.Glu293Asp)
NM_003977.4(AIP):c.887C>A (p.Pro296Gln)
NM_022124.6(CDH23):c.1535C>T (p.Thr512Met)
NM_022124.6(CDH23):c.4195G>A (p.Asp1399Asn)
NM_022124.6(CDH23):c.9726del (p.Ser3243fs)	rs767176528

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