ClinVar Miner

Variants in gene CACNA1G 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
856 80 0 43 21 0 0 63

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.

uncertain significance likely benign benign
uncertain significance 0 16 6
likely benign 16 0 43
benign 6 43 0

All variants with conflicting interpretations #

Total variants: 63
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018896.5(CACNA1G):c.1479C>T (p.His493=) rs9897406 0.02109
NM_018896.5(CACNA1G):c.3993A>C (p.Ala1331=) rs60644455 0.01364
NM_018896.5(CACNA1G):c.1699C>T (p.Arg567Cys) rs60802569 0.01009
NM_018896.5(CACNA1G):c.5601A>G (p.Leu1867=) rs59221624 0.00972
NM_018896.5(CACNA1G):c.5853C>T (p.Asp1951=) rs61467595 0.00707
NM_018896.5(CACNA1G):c.5226+7G>A rs116224642 0.00688
NM_018896.5(CACNA1G):c.7080A>G (p.Lys2360=) rs59256133 0.00599
NM_018896.5(CACNA1G):c.1953C>T (p.Ser651=) rs58348936 0.00590
NM_018896.5(CACNA1G):c.975G>A (p.Ala325=) rs57260523 0.00558
NM_018896.5(CACNA1G):c.1589G>A (p.Arg530His) rs7222276 0.00445
NM_018896.5(CACNA1G):c.3295G>A (p.Ala1099Thr) rs58240016 0.00431
NM_018896.5(CACNA1G):c.1362C>T (p.Val454=) rs116227985 0.00427
NM_018896.5(CACNA1G):c.2907G>A (p.Ala969=) rs60134952 0.00280
NM_018896.5(CACNA1G):c.1925-10C>T rs139447235 0.00240
NM_018896.5(CACNA1G):c.3084C>T (p.His1028=) rs61741117 0.00194
NM_018896.5(CACNA1G):c.4630C>A (p.Arg1544=) rs60532742 0.00161
NM_018896.5(CACNA1G):c.3704G>A (p.Arg1235Gln) rs150972562 0.00160
NM_018896.5(CACNA1G):c.895G>A (p.Gly299Ser) rs201875227 0.00155
NM_018896.5(CACNA1G):c.4084C>T (p.Leu1362=) rs374849749 0.00149
NM_018896.5(CACNA1G):c.2001C>T (p.Cys667=) rs58207445 0.00148
NM_018896.5(CACNA1G):c.3691-6C>G rs182987793 0.00148
NM_018896.5(CACNA1G):c.3111G>A (p.Pro1037=) rs201745304 0.00125
NM_018896.5(CACNA1G):c.858C>A (p.Pro286=) rs56885413 0.00097
NM_018896.5(CACNA1G):c.2069G>A (p.Ser690Asn) rs61453167 0.00087
NM_018896.5(CACNA1G):c.2043C>T (p.Ala681=) rs368524369 0.00082
NM_018896.5(CACNA1G):c.1646G>C (p.Gly549Ala) rs527691624 0.00073
NM_018896.5(CACNA1G):c.1818A>G (p.Ala606=) rs375580888 0.00071
NM_018896.5(CACNA1G):c.1879G>A (p.Gly627Arg) rs200317339 0.00063
NM_018896.5(CACNA1G):c.4155C>G (p.Thr1385=) rs201226731 0.00045
NM_018896.5(CACNA1G):c.6710C>A (p.Pro2237His) rs200141555 0.00039
NM_018896.5(CACNA1G):c.286G>A (p.Val96Met) rs201146969 0.00031
NM_018896.5(CACNA1G):c.6244G>A (p.Val2082Ile) rs752773885 0.00021
NM_018896.5(CACNA1G):c.860C>T (p.Thr287Met) rs200872262 0.00014
NM_018896.5(CACNA1G):c.6077C>T (p.Thr2026Met) rs375919039 0.00011
NM_018896.5(CACNA1G):c.688G>A (p.Val230Ile) rs768796872 0.00009
NM_018896.5(CACNA1G):c.3246G>A (p.Glu1082=) rs769342382 0.00008
NM_018896.5(CACNA1G):c.3010G>A (p.Asp1004Asn) rs377336879 0.00007
NM_018896.5(CACNA1G):c.3553C>T (p.Arg1185Cys) rs573971701 0.00006
NM_018896.5(CACNA1G):c.1556C>T (p.Pro519Leu) rs757227515 0.00005
NM_018896.5(CACNA1G):c.2128A>T (p.Ser710Cys) rs543673731 0.00004
NM_018896.5(CACNA1G):c.305G>A (p.Arg102Gln) rs763813233 0.00003
NM_018896.5(CACNA1G):c.6951G>A (p.Glu2317=) rs544050662 0.00003
NM_018896.5(CACNA1G):c.1588C>T (p.Arg530Cys) rs776897967 0.00002
NM_018896.5(CACNA1G):c.3200G>A (p.Arg1067His) rs369751310 0.00002
NM_018896.5(CACNA1G):c.1633G>C (p.Ala545Pro)
NM_018896.5(CACNA1G):c.1758C>T (p.Ser586=)
NM_018896.5(CACNA1G):c.1777G>A (p.Val593Met)
NM_018896.5(CACNA1G):c.1796C>T (p.Pro599Leu)
NM_018896.5(CACNA1G):c.2014C>T (p.Arg672Trp)
NM_018896.5(CACNA1G):c.2048G>A (p.Arg683His)
NM_018896.5(CACNA1G):c.2454C>T (p.Ser818=)
NM_018896.5(CACNA1G):c.2754+4C>T
NM_018896.5(CACNA1G):c.3065-8C>T
NM_018896.5(CACNA1G):c.3202C>T (p.Arg1068Cys)
NM_018896.5(CACNA1G):c.3265G>A (p.Ala1089Thr)
NM_018896.5(CACNA1G):c.3449G>A (p.Arg1150Gln)
NM_018896.5(CACNA1G):c.354+5GT[16] rs3833150
NM_018896.5(CACNA1G):c.3728G>A (p.Arg1243Gln)
NM_018896.5(CACNA1G):c.4682G>A (p.Arg1561Gln)
NM_018896.5(CACNA1G):c.6181G>A (p.Glu2061Lys)
NM_018896.5(CACNA1G):c.6579G>A (p.Pro2193=) rs57667003
NM_018896.5(CACNA1G):c.7098C>T (p.Ser2366=)
NM_018896.5(CACNA1G):c.78G>A (p.Ser26=) rs577987926

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