ClinVar Miner

Variants in gene RB1 with conflicting interpretations

See also:
Y axis minimum submission review status: Y axis collection method:
X axis minimum submission review status: X axis collection method:
Minimum conflict level:
Gene type:
ClinVar version:

If a variant has more than two submissions, it may have multiple conflicts and therefore be counted in more than one conflict column. If this is the case, the "Variants with any kind of conflict" cell will be less than the sum of the conflicted variants cells to its left.

Variants with only 1 submission per condition Variants with at least 2 submissions on the same condition and no conflicts Variants with a synonymous conflict
(e.g. benign vs non-pathogenic)
Variants with a confidence conflict
(e.g. benign vs likely benign)
Variants with a benign or likely benign vs uncertain conflict Variants with a category conflict
(e.g. benign vs affects)
Variants with a clinically significant conflict
(e.g. benign vs pathogenic)
Variants with any conflict
1251 44 1 29 20 0 3 50

Significance breakdown #

In the table below, cells that correspond to a term paired with itself represent synonymous conflicts, i.e. variants that have been annotated with different terms that map to the same standard term. To compare the terms that were actually submitted, check the box in the filters section at the top of this page.

pathogenic likely pathogenic uncertain significance likely benign benign
pathogenic 0 6 1 1 0
likely pathogenic 6 0 1 0 0
uncertain significance 1 1 1 11 11
likely benign 1 0 11 0 23
benign 0 0 11 23 0

All variants with conflicting interpretations #

Total variants: 50
Download table as spreadsheet
NM_000321.2(RB1):c.1072C>T (p.Arg358Ter) rs121913301
NM_000321.2(RB1):c.1129A>T (p.Thr377Ser) rs146897002
NM_000321.2(RB1):c.1139A>G (p.Asn380Ser) rs1470523018
NM_000321.2(RB1):c.113G>A (p.Gly38Asp) rs766529534
NM_000321.2(RB1):c.1140C>T (p.Asn380=) rs117865557
NM_000321.2(RB1):c.1156A>G (p.Met386Val) rs564780653
NM_000321.2(RB1):c.1216-29A>G rs3092886
NM_000321.2(RB1):c.1306C>A (p.Gln436Lys) rs4151534
NM_000321.2(RB1):c.1363C>T (p.Arg455Ter) rs121913302
NM_000321.2(RB1):c.1390-11A>G rs200658795
NM_000321.2(RB1):c.1573G>A (p.Ala525Thr) rs587778640
NM_000321.2(RB1):c.1574C>G (p.Ala525Gly) rs4151539
NM_000321.2(RB1):c.1707A>G (p.Leu569=) rs3092895
NM_000321.2(RB1):c.1735C>T (p.Arg579Ter) rs121913305
NM_000321.2(RB1):c.1770T>C (p.Cys590=) rs145310579
NM_000321.2(RB1):c.1814+3A>G rs376886420
NM_000321.2(RB1):c.1861C>A (p.Arg621Ser) rs367578442
NM_000321.2(RB1):c.1861C>T (p.Arg621Cys) rs367578442
NM_000321.2(RB1):c.1960G>A (p.Val654Met) rs483352690
NM_000321.2(RB1):c.1966C>T (p.Arg656Trp) rs142509759
NM_000321.2(RB1):c.1967G>A (p.Arg656Gln) rs202031219
NM_000321.2(RB1):c.1973C>A (p.Ala658Asp) rs587778834
NM_000321.2(RB1):c.2003G>A (p.Arg668His) rs551747882
NM_000321.2(RB1):c.2091C>G (p.Asp697Glu) rs3092903
NM_000321.2(RB1):c.2212-16T>A rs201258424
NM_000321.2(RB1):c.2289A>T (p.Arg763Ser) rs1167280920
NM_000321.2(RB1):c.2393G>A (p.Arg798Gln) rs374523971
NM_000321.2(RB1):c.2463A>G (p.Thr821=) rs370088029
NM_000321.2(RB1):c.2521-11G>A rs4151624
NM_000321.2(RB1):c.2652A>C (p.Glu884Asp) rs765537411
NM_000321.2(RB1):c.380+10C>G rs187110786
NM_000321.2(RB1):c.380+12T>C rs3092881
NM_000321.2(RB1):c.397A>C (p.Asn133His) rs3092900
NM_000321.2(RB1):c.411A>T (p.Glu137Asp) rs3092902
NM_000321.2(RB1):c.45_53del (p.Ala16_Ala18del) rs572454921
NM_000321.2(RB1):c.462G>A (p.Lys154=) rs369830657
NM_000321.2(RB1):c.628G>T (p.Asp210Tyr) rs148992508
NM_000321.2(RB1):c.731T>C (p.Ile244Thr) rs147754935
NM_000321.3(RB1):c.1654C>T rs121913303
NM_000321.3(RB1):c.1961-12T>C rs201697122
NM_000321.3(RB1):c.1981C>T rs137853294
NM_000321.3(RB1):c.2360G>A (p.Arg787Gln) rs748094394
NM_000321.3(RB1):c.2518G>A (p.Gly840Arg) rs374157786
NM_000321.3(RB1):c.2566G>A (p.Asp856Asn) rs149359120
NM_000321.3(RB1):c.59C>T (p.Pro20Leu) rs587778637
NM_000321.3(RB1):c.69GCC[3] (p.Pro29del) rs587778823
NM_000321.3(RB1):c.784C>T (p.Arg262Trp) rs556201144
NM_000321.3(RB1):c.920C>T (p.Thr307Ile) rs183898408
NM_000321.3(RB1):c.929G>A (p.Gly310Glu) rs200844292
NM_000321.3(RB1):c.958C>T rs121913300

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