ClinVar Miner

List of variants in gene TDRD5 reported as uncertain significance for not specified

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 61
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001199085.3(TDRD5):c.2302G>A (p.Asp768Asn) rs530274369 0.00051
NM_001199085.3(TDRD5):c.166C>G (p.Leu56Val) rs199604826 0.00019
NM_001199085.3(TDRD5):c.1846G>A (p.Gly616Ser) rs199784694 0.00017
NM_001199085.3(TDRD5):c.2797T>A (p.Ser933Thr) rs145048355 0.00015
NM_001199085.3(TDRD5):c.1490A>T (p.Glu497Val) rs200373683 0.00011
NM_001199085.3(TDRD5):c.344C>T (p.Pro115Leu) rs376799300 0.00011
NM_001199085.3(TDRD5):c.727A>G (p.Thr243Ala) rs200507631 0.00009
NM_001199085.3(TDRD5):c.1795G>A (p.Val599Ile) rs780677767 0.00007
NM_001199085.3(TDRD5):c.2771A>G (p.Gln924Arg) rs140853709 0.00007
NM_001199085.3(TDRD5):c.3099G>A (p.Met1033Ile) rs369126968 0.00006
NM_001199085.3(TDRD5):c.151C>T (p.Arg51Trp) rs138668107 0.00005
NM_001199085.3(TDRD5):c.1402G>C (p.Asp468His) rs777262373 0.00003
NM_001199085.3(TDRD5):c.698C>T (p.Pro233Leu) rs756660429 0.00003
NM_001199085.3(TDRD5):c.1083A>C (p.Gln361His) rs745509164 0.00002
NM_001199085.3(TDRD5):c.1178G>A (p.Arg393Lys) rs1338875656 0.00001
NM_001199085.3(TDRD5):c.1270C>T (p.Pro424Ser) rs201849047 0.00001
NM_001199085.3(TDRD5):c.1355C>T (p.Pro452Leu) rs763278183 0.00001
NM_001199085.3(TDRD5):c.2124A>G (p.Ile708Met) rs1447183181 0.00001
NM_001199085.3(TDRD5):c.218C>A (p.Thr73Asn) rs1427300894 0.00001
NM_001199085.3(TDRD5):c.2260A>T (p.Ser754Cys) rs748677047 0.00001
NM_001199085.3(TDRD5):c.2864A>G (p.Glu955Gly) rs2527243452 0.00001
NM_001199085.3(TDRD5):c.3086G>A (p.Ser1029Asn) rs984019528 0.00001
NM_001199085.3(TDRD5):c.310A>G (p.Met104Val) rs763541638 0.00001
NM_001199085.3(TDRD5):c.499T>A (p.Tyr167Asn) rs2526462675 0.00001
NM_001199085.3(TDRD5):c.574A>G (p.Arg192Gly) rs752790470 0.00001
NM_001199085.3(TDRD5):c.1020T>A (p.Asn340Lys)
NM_001199085.3(TDRD5):c.1190C>G (p.Ser397Cys) rs2526822188
NM_001199085.3(TDRD5):c.1279G>A (p.Val427Met)
NM_001199085.3(TDRD5):c.1418T>C (p.Ile473Thr)
NM_001199085.3(TDRD5):c.1696A>T (p.Ile566Phe) rs2102025801
NM_001199085.3(TDRD5):c.1749G>C (p.Lys583Asn)
NM_001199085.3(TDRD5):c.180G>A (p.Met60Ile) rs758414840
NM_001199085.3(TDRD5):c.182C>T (p.Pro61Leu)
NM_001199085.3(TDRD5):c.1982G>A (p.Arg661Gln)
NM_001199085.3(TDRD5):c.2065G>T (p.Val689Phe) rs1241099149
NM_001199085.3(TDRD5):c.2117G>A (p.Arg706Gln)
NM_001199085.3(TDRD5):c.2129C>T (p.Pro710Leu) rs2526981661
NM_001199085.3(TDRD5):c.2138A>G (p.Lys713Arg)
NM_001199085.3(TDRD5):c.229A>C (p.Lys77Gln)
NM_001199085.3(TDRD5):c.2328G>T (p.Glu776Asp) rs2527048643
NM_001199085.3(TDRD5):c.2549G>C (p.Trp850Ser)
NM_001199085.3(TDRD5):c.2630G>T (p.Gly877Val)
NM_001199085.3(TDRD5):c.2665G>T (p.Gly889Cys) rs766953290
NM_001199085.3(TDRD5):c.2675A>T (p.Asp892Val) rs1223639736
NM_001199085.3(TDRD5):c.2690C>A (p.Pro897His)
NM_001199085.3(TDRD5):c.2704T>C (p.Phe902Leu) rs756995942
NM_001199085.3(TDRD5):c.287G>A (p.Ser96Asn)
NM_001199085.3(TDRD5):c.2904C>G (p.Ser968Arg)
NM_001199085.3(TDRD5):c.2909G>C (p.Arg970Pro) rs748050482
NM_001199085.3(TDRD5):c.3040G>T (p.Ala1014Ser)
NM_001199085.3(TDRD5):c.354T>G (p.His118Gln)
NM_001199085.3(TDRD5):c.355C>T (p.Arg119Trp)
NM_001199085.3(TDRD5):c.373G>A (p.Gly125Arg)
NM_001199085.3(TDRD5):c.47G>A (p.Arg16Lys) rs896902002
NM_001199085.3(TDRD5):c.523A>C (p.Met175Leu)
NM_001199085.3(TDRD5):c.5C>G (p.Ser2Cys)
NM_001199085.3(TDRD5):c.695T>G (p.Phe232Cys) rs750848742
NM_001199085.3(TDRD5):c.704C>T (p.Ala235Val)
NM_001199085.3(TDRD5):c.839A>G (p.Asn280Ser)
NM_001199085.3(TDRD5):c.840C>A (p.Asn280Lys) rs1343188794
NM_001199085.3(TDRD5):c.974T>C (p.Val325Ala)

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.