Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PPP2R1A (Hsa) Molecular Consequence: missense variant
(GRCh38)19:52211400C>T
(Homo sapiens)Allele/Variant
Source: rs571582129
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211400C>T
(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)19:52201979C>T
(Homo sapiens)Allele/Variant
Source: rs775159886
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52201979C>T
(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)19:52213077C>T
(Homo sapiens)Allele/Variant
Source: rs750719391
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213077C>T
(GRCh38)19:52215853T>C
(Homo sapiens)Allele/Variant
Source: rs1357134265
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215853T>C
(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)19:52222246G>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)19:52206024T>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)19:52211274G>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52211274G>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211274G>T
(GRCh38)19:52211322C>T
(Homo sapiens)Allele/Variant
Source: rs868591683
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211322C>T
(GRCh38)19:52211349G>A
(Homo sapiens)Allele/Variant
Source: rs11537700
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211349G>A
(GRCh38)19:52211397G>A
(Homo sapiens)Allele/Variant
Source: rs748386684
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211397G>A
(GRCh38)19:52211451C>T
(Homo sapiens)Allele/Variant
Source: rs763637780
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211451C>T
(GRCh38)19:52211457C>G
(Homo sapiens)Allele/Variant
Source: rs758930597
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211457C>G
(GRCh38)19:52211488C>T
(Homo sapiens)Allele/Variant
Source: rs2122330457
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211488C>T
(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)19:52215829C>T
(Homo sapiens)Allele/Variant
Source: rs1978535720
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215829C>T
(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)19:52190123G>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)19:52211484A>G
(Homo sapiens)Allele/Variant
Source: rs200123377
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211484A>G
(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)19:52212984G>T
(Homo sapiens)Allele/Variant
Source: rs145417094
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212984G>T
(GRCh38)19:52211427G>C
(Homo sapiens)Allele/Variant
Source: rs767340233
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211427G>C
(GRCh38)19:52201938C>G
(Homo sapiens)Allele/Variant
Source: rs771822389
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)19:52201938C>G
(GRCh38)19:52212957C>T
(Homo sapiens)Allele/Variant
Source: rs1371810473
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212957C>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)19:52211310G>A
(Homo sapiens)Allele/Variant
Source: rs1184873116
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211310G>A
(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)19:52202051C>A
(Homo sapiens)Allele/Variant
Source: rs1421549263
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202051C>A
(GRCh38)19:52213056C>T
(Homo sapiens)Allele/Variant
Source: rs756508136
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213056C>T
(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)19:52216515C>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
(GRCh38)19:52216078A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216078A>G
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)19:52216078A>G
(GRCh38)19:52216525C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216525C>G
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)19:52216525C>G
(GRCh38)19:52222261C>T
(Homo sapiens)Allele/Variant
Source: rs1978983800
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222261C>T