Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PPP2R1A (Hsa) Molecular Consequence: non coding transcript variant
(GRCh38)19:52190146T>C
(Homo sapiens)Allele/Variant
Source: rs1290240005
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190146T>C
(GRCh38)19:52216567C>A
(Homo sapiens)Allele/Variant
Source: rs2122350996
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216567C>A
(GRCh38)19:52216591C>G
(Homo sapiens)Allele/Variant
Source: rs749256759
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216591C>G
(GRCh38)19:52220201T>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52220201T>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220201T>C
(GRCh38)19:52220981T>C
(Homo sapiens)Allele/Variant
Source: rs746735616
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220981T>C
(GRCh38)19:52221062A>C
(Homo sapiens)Allele/Variant
Source: rs1978894659
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221062A>C
(GRCh38)19:52202045G>T
(Homo sapiens)Allele/Variant
Source: rs1486590815
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202045G>T
(GRCh38)19:52205951T>C
(Homo sapiens)Allele/Variant
Source: rs768335724
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52205951T>C
(GRCh38)19:52205954G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52205954G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52205954G>A
(GRCh38)19:52215759C>A
(Homo sapiens)Allele/Variant
Source: rs751641627
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215759C>A
(GRCh38)19:52206024T>C
(Homo sapiens)Allele/Variant
Source: rs371261424
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52206024T>C
(GRCh38)19:52201939A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52201939A>G
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52201939A>G
(GRCh38)19:52221086G>A
(Homo sapiens)Allele/Variant
Source: rs969720045
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221086G>A
(GRCh38)19:52225826C>T
(Homo sapiens)Allele/Variant
Source: rs771271451
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225826C>T
(GRCh38)19:52206049G>A
(Homo sapiens)Allele/Variant
Source: rs1377540471
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52206049G>A
(GRCh38)19:52216582C>T
(Homo sapiens)Allele/Variant
Source: rs1334151690
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216582C>T
(GRCh38)19:52221085C>T
(Homo sapiens)Allele/Variant
Source: rs187141962
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221085C>T
(GRCh38)19:52221096A>G
(Homo sapiens)Allele/Variant
Source: rs1285312270
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221096A>G
(GRCh38)19:52221102T>C
(Homo sapiens)Allele/Variant
Source: rs1978897316
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221102T>C
(GRCh38)19:52219852G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52219852G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219852G>A
(GRCh38)19:52212939C>T
(Homo sapiens)Allele/Variant
Source: rs754216175
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212939C>T
(GRCh38)19:52211245G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52211245G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211245G>A
(GRCh38)19:52190111C>G
(Homo sapiens)Allele/Variant
Source: rs2089438141
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190111C>G
(GRCh38)19:52190123G>T
(Homo sapiens)Allele/Variant
Source: rs1420029846
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190123G>T
(GRCh38)19:52201928C>T
(Homo sapiens)Allele/Variant
Source: rs757143630
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52201928C>T
(GRCh38)19:52221065C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52221065C>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221065C>T
(GRCh38)19:52221106C>T
(Homo sapiens)Allele/Variant
Source: rs750426851
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221106C>T
(GRCh38)19:52202050C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52202050C>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202050C>T
(GRCh38)19:52219729C>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52219729C>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219729C>A
(GRCh38)19:52219809A>G
(Homo sapiens)Allele/Variant
Source: rs1447032127
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219809A>G
(GRCh38)19:52190157C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52190157C>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190157C>T
(GRCh38)19:52215775G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52215775G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215775G>A
(GRCh38)19:52220263C>G
(Homo sapiens)Allele/Variant
Source: rs191838323
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220263C>G
(GRCh38)19:52225707C>T
(Homo sapiens)Allele/Variant
Source: rs771075267
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225707C>T
(GRCh38)19:52225708G>A
(Homo sapiens)Allele/Variant
Source: rs1223664301
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225708G>A
(GRCh38)19:52225816C>T
(Homo sapiens)Allele/Variant
Source: rs375739930
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225816C>T
(GRCh38)19:52206025A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52206025A>G
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52206025A>G
(GRCh38)19:52220999G>C
(Homo sapiens)Allele/Variant
Source: rs2122364608
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220999G>C
(GRCh38)19:52221085C>A
(Homo sapiens)Allele/Variant
Source: rs187141962
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221085C>A
(GRCh38)19:52202046G>A
(Homo sapiens)Allele/Variant
Source: rs200369713
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202046G>A
(GRCh38)19:52222246G>A
(Homo sapiens)Allele/Variant
Source: rs1978982927
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222246G>A
(GRCh38)19:52219852G>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52219852G>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219852G>C
(GRCh38)19:52190108C>T
(Homo sapiens)Allele/Variant
Source: rs140334526
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190108C>T
(GRCh38)19:52219679T>G
(Homo sapiens)Allele/Variant
Source: rs1268365200
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219679T>G
(GRCh38)19:52220255T>G
(Homo sapiens)Allele/Variant
Source: rs1372096079
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220255T>G
(GRCh38)19:52190185T>C
(Homo sapiens)Allele/Variant
Source: rs201099965
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190185T>C
(GRCh38)19:52216515C>T
(Homo sapiens)Allele/Variant
Source: rs761860948
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216515C>T
(GRCh38)19:52216524C>G
(Homo sapiens)Allele/Variant
Source: rs1978585374
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216524C>G
(GRCh38)19:52216666A>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216666A>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216666A>C
(GRCh38)19:52212676C>T
(Homo sapiens)Allele/Variant
Source: rs200753254
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212676C>T