ClinVar Miner

Variants in gene ADGRG1 with conflicting interpretations

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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
246 24 0 20 18 0 0 34

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 3 0 0 0
likely pathogenic 3 0 0 0 0
uncertain significance 0 0 0 15 6
likely benign 0 0 15 0 17
benign 0 0 6 17 0

All variants with conflicting interpretations #

Total variants: 34
Download table as spreadsheet
HGVS dbSNP
NM_201525.4(ADGRG1):c.1017+8G>A rs186479054
NM_201525.4(ADGRG1):c.1168-20C>A rs2305309
NM_201525.4(ADGRG1):c.1188C>T (p.Asp396=) rs368883473
NM_201525.4(ADGRG1):c.1191C>T (p.Ala397=) rs1367685651
NM_201525.4(ADGRG1):c.1236C>T (p.Val412=) rs768769972
NM_201525.4(ADGRG1):c.1287-28G>C rs60624815
NM_201525.4(ADGRG1):c.1287-6G>A rs112805221
NM_201525.4(ADGRG1):c.1356G>A (p.Thr452=) rs151020094
NM_201525.4(ADGRG1):c.1460T>C (p.Met487Thr) rs17379472
NM_201525.4(ADGRG1):c.14C>T (p.Ser5Leu) rs147879224
NM_201525.4(ADGRG1):c.1537C>T (p.Leu513=) rs762771228
NM_201525.4(ADGRG1):c.1578G>A (p.Thr526=) rs727503955
NM_201525.4(ADGRG1):c.1665-41C>T rs17240890
NM_201525.4(ADGRG1):c.1675C>T (p.Arg559Trp) rs121908464
NM_201525.4(ADGRG1):c.174C>T (p.Ile58=) rs140963173
NM_201525.4(ADGRG1):c.1781G>A (p.Arg594His) rs757051705
NM_201525.4(ADGRG1):c.1810C>T (p.Leu604=) rs113358058
NM_201525.4(ADGRG1):c.1842C>T (p.Gly614=) rs574553979
NM_201525.4(ADGRG1):c.1933+10A>G rs137936275
NM_201525.4(ADGRG1):c.1952G>A (p.Trp651Ter) rs587783657
NM_201525.4(ADGRG1):c.1983T>C (p.Gly661=) rs111939130
NM_201525.4(ADGRG1):c.2040C>G (p.Gly680=) rs794727146
NM_201525.4(ADGRG1):c.236G>A (p.Arg79Gln) rs13338340
NM_201525.4(ADGRG1):c.243C>T (p.Phe81=) rs58068378
NM_201525.4(ADGRG1):c.26C>T (p.Thr9Met) rs200241873
NM_201525.4(ADGRG1):c.286C>T (p.Arg96Ter) rs146278035
NM_201525.4(ADGRG1):c.401C>T (p.Pro134Leu) rs138344683
NM_201525.4(ADGRG1):c.612C>T (p.Pro204=) rs147495708
NM_201525.4(ADGRG1):c.64+15G>T rs200303272
NM_201525.4(ADGRG1):c.641C>T (p.Ser214Leu) rs114515505
NM_201525.4(ADGRG1):c.66T>G (p.Gly22=) rs369887735
NM_201525.4(ADGRG1):c.843C>G (p.Ser281Arg) rs1801257
NM_201525.4(ADGRG1):c.843_844delinsGC (p.Ser281_Gly282delinsArgArg) rs1057517931
NM_201525.4(ADGRG1):c.996T>C (p.Thr332=) rs1376041

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