List of variants in gene RTTN reported as likely benign for not specified

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: 49

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HGVS	dbSNP	gnomAD frequency
NM_173630.4(RTTN):c.5282T>C (p.Phe1761Ser)	rs4891392	0.79319
NM_173630.4(RTTN):c.376T>G (p.Ser126Ala)	rs3911730	0.73528
NM_173630.4(RTTN):c.734A>G (p.Lys245Arg)	rs17082206	0.40022
NM_173630.4(RTTN):c.6144A>G (p.Val2048=)	rs2304378	0.16509
NM_173630.4(RTTN):c.4940+7G>A	rs17082039	0.02895
NM_173630.4(RTTN):c.4748-5A>G	rs28495061	0.02113
NM_173630.4(RTTN):c.2856A>G (p.Leu952=)	rs35139926	0.02051
NM_173630.4(RTTN):c.2055+7C>T	rs117843366	0.01697
NM_173630.4(RTTN):c.4850T>C (p.Met1617Thr)	rs35409908	0.01493
NM_173630.4(RTTN):c.2886-9A>G	rs75225724	0.01465
NM_173630.4(RTTN):c.1665C>A (p.Asn555Lys)	rs34353615	0.01182
NM_173630.4(RTTN):c.1842A>G (p.Glu614=)	rs140245773	0.01182
NM_173630.4(RTTN):c.5060C>G (p.Ser1687Cys)	rs34717557	0.01180
NM_173630.4(RTTN):c.1008-4G>T	rs151203272	0.01176
NM_173630.4(RTTN):c.841+11T>C	rs114480216	0.00778
NM_173630.4(RTTN):c.6445G>A (p.Ala2149Thr)	rs34989098	0.00624
NM_173630.4(RTTN):c.2466A>G (p.Arg822=)	rs115470168	0.00564
NM_173630.4(RTTN):c.3581A>G (p.Glu1194Gly)	rs34533087	0.00548
NM_173630.4(RTTN):c.183G>A (p.Lys61=)	rs34922729	0.00541
NM_173630.4(RTTN):c.5647+16C>T	rs114315958	0.00541
NM_173630.4(RTTN):c.6636T>C (p.Tyr2212=)	rs35558429	0.00497
NM_173630.4(RTTN):c.227C>T (p.Pro76Leu)	rs114765225	0.00496
NM_173630.4(RTTN):c.4992G>C (p.Leu1664=)	rs34041767	0.00492
NM_173630.4(RTTN):c.5991T>C (p.Pro1997=)	rs34749812	0.00449
NM_173630.4(RTTN):c.2309+12G>A	rs144279235	0.00433
NM_173630.4(RTTN):c.4889G>C (p.Arg1630Thr)	rs182595458	0.00389
NM_173630.4(RTTN):c.635A>C (p.Asp212Ala)	rs12956068	0.00334
NM_173630.4(RTTN):c.5143A>G (p.Asn1715Asp)	rs35374168	0.00275
NM_173630.4(RTTN):c.1330G>A (p.Gly444Arg)	rs199780405	0.00192
NM_173630.4(RTTN):c.885A>G (p.Ala295=)	rs148445363	0.00111
NM_173630.4(RTTN):c.805T>C (p.Phe269Leu)	rs141156594	0.00096
NM_173630.4(RTTN):c.1221A>G (p.Glu407=)	rs112327299	0.00081
NM_173630.4(RTTN):c.3783G>A (p.Pro1261=)	rs371484273	0.00032
NM_173630.4(RTTN):c.2670+9A>G	rs200758402	0.00016
NM_173630.4(RTTN):c.2481+18G>T	rs746996156	0.00012
NM_173630.4(RTTN):c.309T>C (p.Ala103=)	rs554154376	0.00011
NM_173630.4(RTTN):c.4877C>T (p.Thr1626Met)	rs781683199	0.00006
NM_173630.4(RTTN):c.1305+11A>G	rs547572919	0.00003
NM_173630.4(RTTN):c.2520A>C (p.Ser840=)	rs1269456109	0.00001
NM_173630.4(RTTN):c.2789-11T>G	rs1258727329	0.00001
NM_173630.4(RTTN):c.5647+10A>G	rs1057523916	0.00001
NM_173630.4(RTTN):c.2601G>A (p.Val867=)	rs2145715138
NM_173630.4(RTTN):c.27A>G (p.Lys9=)	rs1555784718
NM_173630.4(RTTN):c.3321G>A (p.Lys1107=)	rs147728279
NM_173630.4(RTTN):c.3714A>G (p.Gln1238=)
NM_173630.4(RTTN):c.376T>A (p.Ser126Thr)	rs3911730
NM_173630.4(RTTN):c.5186-4A>G	rs28599773
NM_173630.4(RTTN):c.5323+7_5323+9del	rs770541694
NM_173630.4(RTTN):c.6339C>T (p.His2113=)	rs1201086381

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