List of variants in gene TRPS1 reported by Illumina Laboratory Services, Illumina

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: 21

Download table as spreadsheet

HGVS	dbSNP	gnomAD frequency
NM_014112.5(TRPS1):c.*2537del	rs570702506	0.00088
NM_014112.5(TRPS1):c.2701-9_2701-8del	rs368655299	0.00038
NM_014112.5(TRPS1):c.*338del	rs530055629	0.00035
NM_014112.5(TRPS1):c.-487A>C	rs886062633	0.00010
NM_014112.5(TRPS1):c.2752_2754del	rs886062612	0.00003
NM_014112.5(TRPS1):c.-470T>C	rs567007790	0.00001
NM_014112.5(TRPS1):c.*1843del	rs886062619
NM_014112.5(TRPS1):c.1983_1984insG	rs886062618
NM_014112.5(TRPS1):c.*2740del	rs879823190
NM_014112.5(TRPS1):c.*3538del	rs547899966
NM_014112.5(TRPS1):c.*4593AAAGG[1]	rs755682849
NM_014112.5(TRPS1):c.*4741del	rs886062604
NM_014112.5(TRPS1):c.4754_4761dup	rs755990611
NM_014112.5(TRPS1):c.*4845ATA[1]	rs775143556
NM_014112.5(TRPS1):c.5300_5303del	rs564851438
NM_014112.5(TRPS1):c.-318CT[13]	rs10546472
NM_014112.5(TRPS1):c.-318CT[9]	rs10546472
NM_014112.5(TRPS1):c.-320_-319del	rs199575103
NM_014112.5(TRPS1):c.-382del	rs886062631
NM_014112.5(TRPS1):c.-393_-392dup	rs759303878
NM_014112.5(TRPS1):c.1382C>G (p.Ser461Ter)	rs2130493114

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.