ClinVar Miner

List of variants in gene RET reported as uncertain significance by Genetic Services Laboratory, University of Chicago

Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 21
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HGVS dbSNP gnomAD frequency
NM_020975.6(RET):c.785T>C (p.Val262Ala) rs139790943 0.00025
NM_020975.6(RET):c.2522C>T (p.Pro841Leu) rs149891333 0.00015
NM_020975.6(RET):c.2556C>G (p.Ile852Met) rs377767426 0.00011
NM_020975.6(RET):c.961G>A (p.Gly321Arg) rs377767388 0.00009
NM_020975.6(RET):c.1891G>A (p.Asp631Asn) rs377767406 0.00004
NM_020975.6(RET):c.2371T>A (p.Tyr791Asn) rs377767417 0.00004
NM_020975.6(RET):c.1083C>A (p.Asn361Lys) rs770587835 0.00003
NM_020975.6(RET):c.3113C>T (p.Thr1038Ile) rs200021472 0.00003
NM_020975.6(RET):c.1084C>A (p.Leu362Ile) rs773935854 0.00002
NM_020975.6(RET):c.134C>T (p.Ala45Val) rs763526874 0.00002
NM_020975.6(RET):c.1523-5T>C rs1373899196 0.00002
NM_020975.6(RET):c.3233C>T (p.Thr1078Met) rs762952212 0.00002
NM_020975.6(RET):c.139G>A (p.Gly47Ser) rs529018971 0.00001
NM_020975.6(RET):c.2915G>A (p.Arg972Lys) rs1384605415 0.00001
NM_020975.6(RET):c.3314C>T (p.Ala1105Val) rs532862288 0.00001
NM_020975.6(RET):c.1648+10G>A rs762545740
NM_020975.6(RET):c.1902_1903delinsTT (p.Arg635Cys) rs2132844768
NM_020975.6(RET):c.1934_1936del (p.Ser645del) rs1416677590
NM_020975.6(RET):c.276C>G (p.Thr92=) rs886042820
NM_020975.6(RET):c.2781C>G (p.Ile927Met) rs1838228721
NM_020975.6(RET):c.2935G>A (p.Glu979Lys) rs2133007152

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