List of variants in gene RREB1 reported as benign by Invitae

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: 33

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HGVS	dbSNP	gnomAD frequency
NM_001003699.4(RREB1):c.2343C>T (p.Gly781=)	rs45519731	0.01937
NM_001003699.4(RREB1):c.2948T>C (p.Leu983Ser)	rs115093903	0.01379
NM_001003699.4(RREB1):c.3464G>A (p.Arg1155Gln)	rs35521383	0.00962
NM_001003699.4(RREB1):c.268A>G (p.Thr90Ala)	rs73374662	0.00875
NM_001003699.4(RREB1):c.1024G>A (p.Asp342Asn)	rs113114064	0.00854
NM_001003699.4(RREB1):c.1830G>T (p.Met610Ile)	rs35147576	0.00399
NM_001003699.4(RREB1):c.2397C>T (p.Phe799=)	rs114103178	0.00370
NM_001003699.4(RREB1):c.3974-9G>A	rs149294211	0.00309
NM_001003699.4(RREB1):c.11G>A (p.Ser4Asn)	rs116821447	0.00301
NM_001003699.4(RREB1):c.3189C>T (p.Pro1063=)	rs148116530	0.00295
NM_001003699.4(RREB1):c.87G>A (p.Lys29=)	rs116604236	0.00294
NM_001003699.4(RREB1):c.2229G>A (p.Glu743=)	rs149393874	0.00252
NM_001003699.4(RREB1):c.4953C>T (p.Ala1651=)	rs3734580	0.00229
NM_001003699.4(RREB1):c.3297G>A (p.Thr1099=)	rs116628295	0.00195
NM_001003699.4(RREB1):c.4230G>A (p.Ala1410=)	rs115475946	0.00178
NM_001003699.4(RREB1):c.1659A>G (p.Ser553=)	rs76430868	0.00121
NM_001003699.4(RREB1):c.1713C>G (p.Pro571=)	rs374202026	0.00107
NM_001003699.4(RREB1):c.2862C>T (p.Ser954=)	rs147699375	0.00105
NM_001003699.4(RREB1):c.2955C>T (p.Pro985=)	rs200974282	0.00091
NM_001003699.4(RREB1):c.3045G>A (p.Ala1015=)	rs200845305	0.00049
NM_001003699.4(RREB1):c.4249G>C (p.Asp1417His)	rs776186584	0.00042
NM_001003699.4(RREB1):c.2574C>G (p.Pro858=)	rs116759588	0.00038
NM_001003699.4(RREB1):c.6G>A (p.Thr2=)	rs149124719	0.00022
NM_001003699.4(RREB1):c.1642A>C (p.Lys548Gln)	rs116672033	0.00021
NM_001003699.4(RREB1):c.3678C>T (p.Pro1226=)	rs200374066	0.00007
NM_001003699.4(RREB1):c.4986T>C (p.Asn1662=)	rs574936730	0.00005
NM_001003699.4(RREB1):c.846C>T (p.His282=)	rs115003447	0.00005
NM_001003699.4(RREB1):c.2514C>T (p.Ala838=)	rs201261986	0.00004
NM_001003699.4(RREB1):c.2877T>G (p.Pro959=)	rs547655770	0.00003
NM_001003699.4(RREB1):c.4307C>T (p.Ala1436Val)	rs533475141	0.00003
NM_001003699.4(RREB1):c.132G>A (p.Ser44=)	rs200955755	0.00001
NM_001003699.4(RREB1):c.1212C>T (p.Pro404=)	rs142150270
NM_001003699.4(RREB1):c.4311C>T (p.Gly1437=)	rs187908583

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