ClinVar Miner

List of variants in gene RET reported as pathogenic for adrenal carcinoma

Included ClinVar conditions (8):
Minimum submission review status: Collection method:
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Gene type:
ClinVar version:
Total variants: 54
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HGVS dbSNP
NM_020630.5(RET):c.[1901G>A;2121T>A]
NM_020975.4(RET):c.1891G>T(;)2372A>T
NM_020975.4(RET):c.1891G>T(;)2456G>T(;)2529G>T
NM_020975.4(RET):c.[1859G>T;2372A>T]
NM_020975.4(RET):c.[1896G>C;1897C>G;1900T>C]
NM_020975.4(RET):c.[1900T>C;1919C>G;2098A>T]
NM_020975.4(RET):c.[1901G>A;2556C>G]
NM_020975.4(RET):c.[1901G>C;1921G>T]
NM_020975.4(RET):c.[2342A>G;2410G>A]
NM_020975.4(RET):c.[2372A>T;2753T>C]
NM_020975.4(RET):c.[2410G>A;2413G>A]
NM_020975.4(RET):c.[2410G>A;2417A>G]
NM_020975.4(RET):c.[2410G>A;2711C>G]
NM_020975.4(RET):c.[2753T>C;2765C>A]
NM_020975.4:c.[1900T>C];[1946C>T]
NM_020975.4:c.[1902C>G];[1946C>T]
NM_020975.4:c.[1942G>A];[2410G>C]
NM_020975.6(RET):c.1513_1518del (p.Glu505_Gly506del) rs1554818555
NM_020975.6(RET):c.1825T>G (p.Cys609Gly) rs77558292
NM_020975.6(RET):c.1826G>A (p.Cys609Tyr) rs77939446
NM_020975.6(RET):c.1826G>C (p.Cys609Ser) rs77939446
NM_020975.6(RET):c.1833C>G (p.Cys611Trp) rs80069458
NM_020975.6(RET):c.1852T>C (p.Cys618Arg) rs76262710
NM_020975.6(RET):c.1852T>G (p.Cys618Gly) rs76262710
NM_020975.6(RET):c.1853G>C (p.Cys618Ser) rs79781594
NM_020975.6(RET):c.1857_1858delinsTC (p.Cys620Arg) rs1554818784
NM_020975.6(RET):c.1858T>C (p.Cys620Arg) rs77316810
NM_020975.6(RET):c.1858T>G (p.Cys620Gly) rs77316810
NM_020975.6(RET):c.1859G>A (p.Cys620Tyr) rs77503355
NM_020975.6(RET):c.1859G>T (p.Cys620Phe) rs77503355
NM_020975.6(RET):c.1890_1892CGA[1] (p.Asp631del) rs377767435
NM_020975.6(RET):c.1891G>T (p.Asp631Tyr) rs377767406
NM_020975.6(RET):c.1892_1903dup (p.Arg635_Thr636insHisGluLeuCys) rs377767436
NM_020975.6(RET):c.1900T>C (p.Cys634Arg) rs75076352
NM_020975.6(RET):c.1900T>G (p.Cys634Gly) rs75076352
NM_020975.6(RET):c.1900_1908dup (p.Cys634_Thr636dup) rs377767437
NM_020975.6(RET):c.1901G>A (p.Cys634Tyr) rs75996173
NM_020975.6(RET):c.1901G>C (p.Cys634Ser) rs75996173
NM_020975.6(RET):c.1901G>T (p.Cys634Phe) rs75996173
NM_020975.6(RET):c.1901_1902delinsTG (p.Cys634Leu) rs377767409
NM_020975.6(RET):c.1902C>G (p.Cys634Trp) rs77709286
NM_020975.6(RET):c.1919C>G (p.Ala640Gly) rs78935588
NM_020975.6(RET):c.1942G>A (p.Val648Ile) rs77711105
NM_020975.6(RET):c.1997A>C (p.Lys666Thr) rs377767439
NM_020975.6(RET):c.1998G>T (p.Lys666Asn) rs146646971
NM_020975.6(RET):c.2121T>A (p.Asp707Glu) rs1554818959
NM_020975.6(RET):c.2370G>C (p.Leu790Phe) rs75030001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe) rs75030001
NM_020975.6(RET):c.2410G>A (p.Val804Met) rs79658334
NM_020975.6(RET):c.2410G>T (p.Val804Leu) rs79658334
NM_020975.6(RET):c.2647_2648delinsTT (p.Ala883Phe) rs377767429
NM_020975.6(RET):c.2671T>G (p.Ser891Ala) rs75234356
NM_020975.6(RET):c.2753T>C (p.Met918Thr) rs74799832
NM_020975.6(RET):c.874G>A (p.Val292Met) rs34682185

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