ClinVar Miner

List of variants in gene TCOF1 reported as likely benign by PreventionGenetics, part of Exact Sciences

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Total variants: 46
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HGVS dbSNP gnomAD frequency
NM_001371623.1(TCOF1):c.3623T>A (p.Met1208Lys) rs139081024 0.00114
NM_001371623.1(TCOF1):c.1034A>G (p.Glu345Gly) rs150637771 0.00102
NM_001371623.1(TCOF1):c.1864G>A (p.Glu622Lys) rs144872197 0.00057
NM_001371623.1(TCOF1):c.1390G>A (p.Ala464Thr) rs150956690 0.00051
NM_001371623.1(TCOF1):c.2731G>T (p.Ala911Ser) rs557426457 0.00041
NM_001371623.1(TCOF1):c.2248A>G (p.Thr750Ala) rs149384321 0.00039
NM_001371623.1(TCOF1):c.1217G>A (p.Arg406Gln) rs140204483 0.00034
NM_001371623.1(TCOF1):c.2000G>A (p.Arg667Gln) rs146735293 0.00032
NM_001371623.1(TCOF1):c.1547C>T (p.Pro516Leu) rs138645438 0.00028
NM_001371623.1(TCOF1):c.2332C>T (p.Pro778Ser) rs368225177 0.00026
NM_001371623.1(TCOF1):c.3191A>G (p.Lys1064Arg) rs149117118 0.00025
NM_001371623.1(TCOF1):c.3493G>C (p.Gly1165Arg) rs141095369 0.00018
NM_001371623.1(TCOF1):c.188G>A (p.Arg63Gln) rs371609378 0.00014
NM_001371623.1(TCOF1):c.1545G>T (p.Gly515=) rs374664344 0.00012
NM_001371623.1(TCOF1):c.3785G>T (p.Gly1262Val) rs375337164 0.00011
NM_001371623.1(TCOF1):c.270G>A (p.Glu90=) rs777057497 0.00008
NM_001371623.1(TCOF1):c.630A>G (p.Thr210=) rs765654624 0.00005
NM_001371623.1(TCOF1):c.633C>T (p.Asp211=) rs750978663 0.00005
NM_001371623.1(TCOF1):c.187C>T (p.Arg63Trp) rs367964727 0.00004
NM_001371623.1(TCOF1):c.1923C>T (p.Thr641=) rs781033363 0.00002
NM_001371623.1(TCOF1):c.1867G>A (p.Ala623Thr) rs201126288 0.00001
NM_001371623.1(TCOF1):c.3518-3C>T rs543072968 0.00001
NM_001371623.1(TCOF1):c.449A>G (p.Asn150Ser) rs141805606 0.00001
NM_001371623.1(TCOF1):c.723C>A (p.Ala241=) rs763497947 0.00001
NM_001371623.1(TCOF1):c.1128C>A (p.Ala376=) rs149825269
NM_001371623.1(TCOF1):c.1353T>G (p.Ala451=)
NM_001371623.1(TCOF1):c.1413G>A (p.Gln471=)
NM_001371623.1(TCOF1):c.1564G>A (p.Gly522Ser)
NM_001371623.1(TCOF1):c.1629G>A (p.Glu543=)
NM_001371623.1(TCOF1):c.1791C>T (p.Val597=)
NM_001371623.1(TCOF1):c.2000G>C (p.Arg667Pro) rs146735293
NM_001371623.1(TCOF1):c.207G>A (p.Ala69=)
NM_001371623.1(TCOF1):c.2781G>A (p.Gly927=)
NM_001371623.1(TCOF1):c.2838G>A (p.Pro946=)
NM_001371623.1(TCOF1):c.3282C>G (p.Thr1094=)
NM_001371623.1(TCOF1):c.3375C>T (p.Leu1125=)
NM_001371623.1(TCOF1):c.3450C>T (p.Ser1150=)
NM_001371623.1(TCOF1):c.3546C>T (p.Thr1182=)
NM_001371623.1(TCOF1):c.381A>G (p.Ala127=)
NM_001371623.1(TCOF1):c.3873G>A (p.Ala1291=)
NM_001371623.1(TCOF1):c.4087AAG[4] (p.Lys1367del) rs773205979
NM_001371623.1(TCOF1):c.566-10C>T
NM_001371623.1(TCOF1):c.714G>A (p.Ala238=)
NM_001371623.1(TCOF1):c.771G>A (p.Leu257=)
NM_001371623.1(TCOF1):c.827_844del (p.Gly276_Glu281del) rs528897827
NM_001371623.1(TCOF1):c.930C>G (p.Thr310=)

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