ClinVar Miner

Variants in gene GALT with conflicting interpretations

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 Variants with at least 2 submissions 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 kind of conflict
273 47 3 56 5 3 49 103

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 other
pathogenic 0 48 38 1 3 2
likely pathogenic 48 0 14 0 2 0
uncertain significance 38 14 2 4 1 0
likely benign 1 0 4 1 8 2
benign 3 2 1 8 0 3
other 2 0 0 2 3 0

All variants with conflicting interpretations #

Total variants: 103
Download table as spreadsheet
HGVS dbSNP
NM_000155.2(GALT):c.-119_-116delGTCA rs111033640
NM_000155.3(GALT):c.1006A>T (p.Met336Leu) rs111033810
NM_000155.3(GALT):c.100T>A (p.Tyr34Asn) rs111033836
NM_000155.3(GALT):c.1014C>G (p.Gly338=) rs111033811
NM_000155.3(GALT):c.1030C>A (p.Gln344Lys) rs111033814
NM_000155.3(GALT):c.1052delC (p.Pro351Leufs) rs111033813
NM_000155.3(GALT):c.1057C>T (p.Gln353Ter) rs111033818
NM_000155.3(GALT):c.1059+24G>A rs111033840
NM_000155.3(GALT):c.1060-1G>A rs367543268
NM_000155.3(GALT):c.107C>T (p.Pro36Leu) rs111033645
NM_000155.3(GALT):c.1140A>C (p.Ter380Cys) rs111033827
NM_000155.3(GALT):c.134C>T (p.Ser45Leu) rs111033652
NM_000155.3(GALT):c.152G>A (p.Arg51Gln) rs111033648
NM_000155.3(GALT):c.157T>A (p.Trp53Arg) rs1131691837
NM_000155.3(GALT):c.18delC (p.Asp7Ilefs) rs111033638
NM_000155.3(GALT):c.197C>T (p.Pro66Leu) rs111033656
NM_000155.3(GALT):c.238C>T (p.Arg80Ter) rs111033664
NM_000155.3(GALT):c.241G>A (p.Ala81Thr) rs111033665
NM_000155.3(GALT):c.247G>A (p.Gly83Arg) rs111033660
NM_000155.3(GALT):c.25C>T (p.Gln9Ter) rs111033848
NM_000155.3(GALT):c.27G>C (p.Gln9His) rs111033637
NM_000155.3(GALT):c.292G>A (p.Asp98Asn) rs111033670
NM_000155.3(GALT):c.292G>C (p.Asp98His) rs111033670
NM_000155.3(GALT):c.307C>T (p.Gln103Ter) rs1225091358
NM_000155.3(GALT):c.329G>A (p.Gly110Glu) rs1057523885
NM_000155.3(GALT):c.367C>G (p.Arg123Gly) rs111033674
NM_000155.3(GALT):c.379A>G (p.Lys127Glu) rs111033682
NM_000155.3(GALT):c.389G>A (p.Cys130Tyr) rs367543255
NM_000155.3(GALT):c.394C>T (p.His132Tyr) rs111033688
NM_000155.3(GALT):c.396C>A (p.His132Gln) rs367543256
NM_000155.3(GALT):c.404C>G (p.Ser135Trp) rs111033690
NM_000155.3(GALT):c.404C>T (p.Ser135Leu) rs111033690
NM_000155.3(GALT):c.413C>T (p.Thr138Met) rs111033686
NM_000155.3(GALT):c.414G>T (p.Thr138=) rs116479817
NM_000155.3(GALT):c.41delCinsTT (p.Ala14Valfs) rs111033634
NM_000155.3(GALT):c.443G>A (p.Arg148Gln) rs111033694
NM_000155.3(GALT):c.450T>A (p.Val150=) rs886063884
NM_000155.3(GALT):c.496C>G (p.Pro166Ala) rs367543257
NM_000155.3(GALT):c.502G>T (p.Val168Leu) rs367543258
NM_000155.3(GALT):c.508-1G>C rs398123181
NM_000155.3(GALT):c.508-29delT rs111033711
NM_000155.3(GALT):c.510C>A (p.Ile170=) rs61735984
NM_000155.3(GALT):c.512T>C (p.Phe171Ser) rs111033715
NM_000155.3(GALT):c.547C>A (p.Pro183Thr) rs111033721
NM_000155.3(GALT):c.552C>A (p.His184Gln) rs111033717
NM_000155.3(GALT):c.554C>T (p.Pro185Leu) rs111033722
NM_000155.3(GALT):c.564+15G>A rs111033732
NM_000155.3(GALT):c.564+1G>A rs111033723
NM_000155.3(GALT):c.564+7G>A rs760189807
NM_000155.3(GALT):c.565-2A>G rs111033731
NM_000155.3(GALT):c.572C>T (p.Ala191Val) rs794727838
NM_000155.3(GALT):c.598delC (p.Gln200Serfs) rs111033738
NM_000155.3(GALT):c.602G>A (p.Arg201His) rs111033735
NM_000155.3(GALT):c.607G>A (p.Glu203Lys) rs111033736
NM_000155.3(GALT):c.610C>T (p.Arg204Ter) rs111033737
NM_000155.3(GALT):c.619C>T (p.Gln207Ter) rs111033743
NM_000155.3(GALT):c.626A>G (p.Tyr209Cys) rs111033744
NM_000155.3(GALT):c.634C>T (p.Gln212Ter) rs111033746
NM_000155.3(GALT):c.652C>G (p.Leu218Val) rs2070075
NM_000155.3(GALT):c.652C>T (p.Leu218=) rs2070075
NM_000155.3(GALT):c.652delC (p.Leu218Terfs) rs111033742
NM_000155.3(GALT):c.676C>G (p.Leu226Val) rs111033751
NM_000155.3(GALT):c.687+9G>C rs117998880
NM_000155.3(GALT):c.688-2A>C rs398123185
NM_000155.3(GALT):c.691C>T (p.Arg231Cys) rs111033749
NM_000155.3(GALT):c.752A>C (p.Tyr251Ser) rs111033755
NM_000155.3(GALT):c.752A>G (p.Tyr251Cys) rs111033755
NM_000155.3(GALT):c.753C>T (p.Tyr251=) rs367543261
NM_000155.3(GALT):c.772C>T (p.Arg258Cys) rs368166217
NM_000155.3(GALT):c.775C>T (p.Arg259Trp) rs786204763
NM_000155.3(GALT):c.776G>A (p.Arg259Gln) rs886042070
NM_000155.3(GALT):c.779_790delATGTGCGGCGGC (p.His260_Arg263del) rs111033762
NM_000155.3(GALT):c.790_792invCTA (p.Leu264Ter)
NM_000155.3(GALT):c.793C>G (p.Pro265Ala) rs111033764
NM_000155.3(GALT):c.814C>T (p.Arg272Cys) rs111033766
NM_000155.3(GALT):c.815G>A (p.Arg272His) rs111033831
NM_000155.3(GALT):c.820+13A>G rs111033768
NM_000155.3(GALT):c.821-46G>T rs111033776
NM_000155.3(GALT):c.82G>A (p.Asp28Asn) rs111033636
NM_000155.3(GALT):c.844C>G (p.Leu282Val) rs111033772
NM_000155.3(GALT):c.857A>G (p.Tyr286Cys) rs367543262
NM_000155.3(GALT):c.876G>A (p.Thr292=) rs1055607
NM_000155.3(GALT):c.883C>A (p.Pro295Thr) rs111033783
NM_000155.3(GALT):c.893T>C (p.Met298Thr) rs886042064
NM_000155.3(GALT):c.91C>A (p.His31Asn) rs111033643
NM_000155.3(GALT):c.938G>A (p.Trp313Ter) rs1410159094
NM_000155.3(GALT):c.940A>G (p.Asn314Asp) rs2070074
NM_000155.3(GALT):c.945T>C (p.His315=) rs61735982
NM_000155.3(GALT):c.947G>A (p.Trp316Ter) rs111033790
NM_000155.3(GALT):c.957C>A (p.His319Gln) rs111033792
NM_000155.3(GALT):c.957C>T (p.His319=) rs111033792
NM_000155.3(GALT):c.958G>A (p.Ala320Thr) rs111033795
NM_000155.3(GALT):c.961C>T (p.His321Tyr) rs367543266
NM_000155.3(GALT):c.970C>T (p.Pro324Ser) rs111033798
NM_000155.3(GALT):c.974C>T (p.Pro325Leu) rs111033794
NM_000155.3(GALT):c.982C>T (p.Arg328Cys) rs144993986
NM_000155.3(GALT):c.983G>A (p.Arg328His) rs111033802
NM_000155.3(GALT):c.98G>A (p.Arg33His) rs111033829
NM_000155.3(GALT):c.997C>T (p.Arg333Trp) rs111033800
NM_000155.3(GALT):c.998G>A (p.Arg333Gln) rs111033808
NM_001258332.1(GALT):c.125T>C (p.Val42Ala) rs111033701
NM_001258332.1(GALT):c.485A>G (p.Glu162Gly) rs111033765
NM_001258332.1(GALT):c.805A>G (p.Ile269Val) rs111033819

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