List of variants in gene TTC21B reported by Genetic Services Laboratory, University of Chicago

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 26

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_024753.5(TTC21B):c.826A>G (p.Thr276Ala)	rs7592429	0.95088
NM_024753.5(TTC21B):c.601G>A (p.Val201Met)	rs1432273	0.61903
NM_024753.5(TTC21B):c.1695C>T (p.Tyr565=)	rs6750044	0.34586
NM_024753.5(TTC21B):c.2175T>C (p.Phe725=)	rs10176588	0.33260
NM_024753.5(TTC21B):c.1417C>T (p.Leu473Phe)	rs2163649	0.01776
NM_024753.5(TTC21B):c.2334C>T (p.Tyr778=)	rs79656636	0.01606
NM_024753.5(TTC21B):c.1387C>T (p.Pro463Ser)	rs16851307	0.01408
NM_024753.5(TTC21B):c.2385G>C (p.Leu795=)	rs80225158	0.01377
NM_024753.5(TTC21B):c.665A>T (p.Gln222Leu)	rs80026831	0.01296
NM_024753.5(TTC21B):c.838A>G (p.Met280Val)	rs112868646	0.01295
NM_024753.5(TTC21B):c.2742C>T (p.Cys914=)	rs73018799	0.01072
NM_024753.5(TTC21B):c.724G>A (p.Asp242Asn)	rs74447004	0.00356
NM_024753.5(TTC21B):c.1846C>T (p.Arg616Cys)	rs139441507	0.00235
NM_024753.5(TTC21B):c.2600G>A (p.Arg867His)	rs76726265	0.00161
NM_024753.5(TTC21B):c.1867T>C (p.Leu623=)	rs140107312	0.00129
NM_024753.5(TTC21B):c.2161A>C (p.Asn721His)	rs146637219	0.00124
NM_024753.5(TTC21B):c.2472G>A (p.Leu824=)	rs114725374	0.00107
NM_024753.5(TTC21B):c.691A>T (p.Thr231Ser)	rs149925563	0.00071
NM_024753.5(TTC21B):c.3797C>T (p.Pro1266Leu)	rs140384742	0.00054
NM_024753.5(TTC21B):c.3914A>G (p.Asp1305Gly)	rs147540469	0.00031
NM_024753.5(TTC21B):c.1448C>A (p.Thr483Asn)	rs142887208	0.00016
NM_024753.5(TTC21B):c.2500C>T (p.Gln834Ter)	rs79746977	0.00009
NM_024753.5(TTC21B):c.455A>C (p.Asp152Ala)	rs145726127	0.00006
NM_024753.5(TTC21B):c.114C>G (p.Val38=)	rs34486024
NM_024753.5(TTC21B):c.3021_3025dup (p.Phe1009fs)	rs1553506928
NM_024753.5(TTC21B):c.3519T>C (p.Thr1173=)	rs115504901

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.