ClinVar Miner

List of variants in gene TRAPPC11 reported as uncertain significance by Athena Diagnostics Inc

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 16
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HGVS dbSNP gnomAD frequency
NM_021942.6(TRAPPC11):c.931C>G (p.Leu311Val) rs148833310 0.00057
NM_021942.6(TRAPPC11):c.1901A>G (p.Asn634Ser) rs148567547 0.00026
NM_021942.6(TRAPPC11):c.1894-10C>T rs111381550 0.00024
NM_021942.6(TRAPPC11):c.3400T>C (p.Ter1134Arg) rs142222368 0.00021
NM_021942.6(TRAPPC11):c.3211G>A (p.Gly1071Ser) rs141588557 0.00007
NM_021942.6(TRAPPC11):c.2234C>A (p.Thr745Lys) rs768000138 0.00004
NM_021942.6(TRAPPC11):c.3194G>A (p.Arg1065Gln) rs567387885 0.00004
NM_021942.6(TRAPPC11):c.1349G>A (p.Arg450Gln) rs201387237 0.00001
NM_021942.6(TRAPPC11):c.2093G>A (p.Cys698Tyr) rs773726834 0.00001
NM_021942.6(TRAPPC11):c.248C>G (p.Thr83Ser) rs1024182354 0.00001
NM_021942.6(TRAPPC11):c.3236A>G (p.Asn1079Ser) rs898762603 0.00001
NM_021942.6(TRAPPC11):c.1972T>A (p.Cys658Ser) rs1215126741
NM_021942.6(TRAPPC11):c.2574T>C (p.Ser858=)
NM_021942.6(TRAPPC11):c.2814G>C (p.Met938Ile) rs1554010787
NM_021942.6(TRAPPC11):c.69G>A (p.Thr23=)
NM_021942.6(TRAPPC11):c.835T>C (p.Cys279Arg)

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