List of variants in gene RET reported as pathogenic for carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 84

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HGVS	dbSNP	gnomAD frequency
NM_020975.6(RET):c.2372A>T (p.Tyr791Phe)	rs77724903	0.00178
NM_020975.6(RET):c.2410G>A (p.Val804Met)	rs79658334	0.00022
NM_020975.6(RET):c.1942G>A (p.Val648Ile)	rs77711105	0.00007
NM_020975.6(RET):c.1998G>T (p.Lys666Asn)	rs146646971	0.00003
NM_020975.6(RET):c.1826G>A (p.Cys609Tyr)	rs77939446	0.00001
NM_020975.6(RET):c.1900T>C (p.Cys634Arg)	rs75076352	0.00001
NM_020975.6(RET):c.1996A>G (p.Lys666Glu)	rs143795581	0.00001
NM_020975.6(RET):c.2370G>T (p.Leu790Phe)	rs75030001	0.00001
NM_020975.6(RET):c.2671T>G (p.Ser891Ala)	rs75234356	0.00001
NM_020975.4(RET):c.[1896G>C;1897C>G;1900T>C]
NM_020975.4(RET):c.[2410G>A;2711C>G]
NM_020975.4(RET):c.[2410G>A;2832C>G]
NM_020975.6(RET):c.1001G>A (p.Trp334Ter)
NM_020975.6(RET):c.1044_1051dup (p.Val351fs)
NM_020975.6(RET):c.1091_1104del (p.Ile364fs)
NM_020975.6(RET):c.1151del (p.Pro384fs)	rs1837854100
NM_020975.6(RET):c.1160del (p.Gly387fs)
NM_020975.6(RET):c.1252C>T (p.Arg418Ter)	rs2132747295
NM_020975.6(RET):c.1315C>T (p.Gln439Ter)	rs2132767341
NM_020975.6(RET):c.1347C>A (p.Cys449Ter)
NM_020975.6(RET):c.1471C>T (p.Gln491Ter)	rs1397494237
NM_020975.6(RET):c.1495C>T (p.Gln499Ter)
NM_020975.6(RET):c.1586_1594dup (p.Cys531_Gly532insGluGluCys)	rs377767434
NM_020975.6(RET):c.1597G>T (p.Gly533Cys)	rs75873440
NM_020975.6(RET):c.1698del (p.Asp567fs)
NM_020975.6(RET):c.1783G>T (p.Glu595Ter)	rs1483605155
NM_020975.6(RET):c.1825T>C (p.Cys609Arg)	rs77558292
NM_020975.6(RET):c.1825T>G (p.Cys609Gly)	rs77558292
NM_020975.6(RET):c.1826G>C (p.Cys609Ser)	rs77939446
NM_020975.6(RET):c.1826G>T (p.Cys609Phe)	rs77939446
NM_020975.6(RET):c.1831T>A (p.Cys611Ser)	rs377767391
NM_020975.6(RET):c.1831T>C (p.Cys611Arg)	rs377767391
NM_020975.6(RET):c.1832G>A (p.Cys611Tyr)	rs377767397
NM_020975.6(RET):c.1832G>T (p.Cys611Phe)	rs377767397
NM_020975.6(RET):c.1832_1833delinsAT (p.Cys611Tyr)	rs377767398
NM_020975.6(RET):c.1833C>G (p.Cys611Trp)	rs80069458
NM_020975.6(RET):c.1852T>A (p.Cys618Ser)	rs76262710
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>A (p.Cys618Tyr)	rs79781594
NM_020975.6(RET):c.1853G>C (p.Cys618Ser)	rs79781594
NM_020975.6(RET):c.1853G>T (p.Cys618Phe)	rs79781594
NM_020975.6(RET):c.1858T>A (p.Cys620Ser)	rs77316810
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>C (p.Cys620Ser)	rs77503355
NM_020975.6(RET):c.1859G>T (p.Cys620Phe)	rs77503355
NM_020975.6(RET):c.1860C>G (p.Cys620Trp)	rs79890926
NM_020975.6(RET):c.1888T>C (p.Cys630Arg)	rs377767404
NM_020975.6(RET):c.1889G>A (p.Cys630Tyr)	rs377767405
NM_020975.6(RET):c.1891G>T (p.Asp631Tyr)	rs377767406
NM_020975.6(RET):c.1899_1900delinsTC (p.Cys634Arg)
NM_020975.6(RET):c.1900T>A (p.Cys634Ser)	rs75076352
NM_020975.6(RET):c.1900T>G (p.Cys634Gly)	rs75076352
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_1902delinsTT (p.Cys634Phe)
NM_020975.6(RET):c.1902C>G (p.Cys634Trp)	rs77709286
NM_020975.6(RET):c.1902_1903inv (p.Cys634_Arg635delinsTrpGly)
NM_020975.6(RET):c.1919C>G (p.Ala640Gly)	rs78935588
NM_020975.6(RET):c.1956_1965delinsACCACTCTACCACAAGTT (p.Ser653fs)
NM_020975.6(RET):c.1998G>C (p.Lys666Asn)	rs146646971
NM_020975.6(RET):c.229C>T (p.Arg77Cys)	rs1588862595
NM_020975.6(RET):c.2304G>C (p.Glu768Asp)	rs78014899
NM_020975.6(RET):c.2304G>T (p.Glu768Asp)	rs78014899
NM_020975.6(RET):c.2304_2307delinsCCTT (p.Glu768Asp)
NM_020975.6(RET):c.2370G>C (p.Leu790Phe)	rs75030001
NM_020975.6(RET):c.2410G>C (p.Val804Leu)	rs79658334
NM_020975.6(RET):c.2410G>T (p.Val804Leu)	rs79658334
NM_020975.6(RET):c.2427C>A (p.Tyr809Ter)	rs577929869
NM_020975.6(RET):c.255G>A (p.Trp85Ter)
NM_020975.6(RET):c.2631del (p.Arg878fs)	rs1838178970
NM_020975.6(RET):c.2647_2648delinsTT (p.Ala883Phe)	rs377767429
NM_020975.6(RET):c.2689C>T (p.Arg897Ter)	rs1060500759
NM_020975.6(RET):c.268G>T (p.Glu90Ter)	rs1588862638
NM_020975.6(RET):c.2735G>C (p.Arg912Pro)	rs78347871
NM_020975.6(RET):c.2753T>C (p.Met918Thr)	rs74799832
NM_020975.6(RET):c.2865dup (p.Pro956fs)	rs1564500612
NM_020975.6(RET):c.317G>A (p.Trp106Ter)	rs2132664970
NM_020975.6(RET):c.318G>A (p.Trp106Ter)	rs2132664999
NM_020975.6(RET):c.538C>T (p.Arg180Ter)	rs76449634
NM_020975.6(RET):c.936_939del (p.Arg312fs)	rs1837778621

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