ClinVar Miner

List of variants in gene SYCP3 studied for spermatogenic failure

Included ClinVar conditions (116):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 15
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001177949.2(SYCP3):c.-122T>A rs17031944 0.02365
NM_001177949.2(SYCP3):c.435A>G (p.Glu145=) rs78591432 0.01236
NM_001177949.2(SYCP3):c.-53C>G rs137993065 0.00185
NM_001177949.2(SYCP3):c.-74T>C rs541789192 0.00042
NM_001177949.2(SYCP3):c.59A>G (p.Gln20Arg) rs143228358 0.00020
NM_001177949.2(SYCP3):c.80T>C (p.Phe27Ser) rs193241367 0.00012
NM_001177949.2(SYCP3):c.657T>C (p.Thr219=) rs769825641 0.00006
NM_001177949.2(SYCP3):c.-64C>T rs886048840 0.00001
NM_001177949.2(SYCP3):c.-106A>G rs143456701
NM_001177949.2(SYCP3):c.28A>T (p.Arg10Trp) rs1952523498
NM_001177949.2(SYCP3):c.454-13_454-9del rs145003954
NM_001177949.2(SYCP3):c.484C>T (p.Gln162Ter)
NM_001177949.2(SYCP3):c.524_527del (p.Ile175fs) rs749759423
NM_001177949.2(SYCP3):c.553-21_553-18del rs587776620
NM_001177949.2(SYCP3):c.643del (p.Ile215fs)

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.