Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PPP2R1A (Hsa)
(GRCh38)19:52211264C>T
(Homo sapiens)Allele/Variant
Source: rs950558629
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211264C>T
(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)19:52211389C>T
(Homo sapiens)Allele/Variant
Source: rs546812521
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211389C>T
(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)19:52216543T>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216543T>G
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216543T>G
(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)19:52222127T>C
(Homo sapiens)Allele/Variant
Source: rs778543586
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222127T>C
(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)19:52206024T>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)19:52211461G>C
(Homo sapiens)Allele/Variant
Source: rs2122330245
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211461G>C
(GRCh38)19:52211473G>A
(Homo sapiens)Allele/Variant
Source: rs146859239
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52211473G>A
(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)19:52212939C>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)19:52211484A>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)19:52215875G>A
(Homo sapiens)Allele/Variant
Source: rs2122348708
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215875G>A
(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)19:52190157C>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)19:52225802C>A
(Homo sapiens)Allele/Variant
Source: rs1379445826
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225802C>A
(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)19:52211310G>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)19:52220999G>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)19:52221062A>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)19:52212721T>C
(Homo sapiens)Allele/Variant
Source: rs1600167941
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
Diseases: Not Available
Variant Name: (GRCh38)19:52212721T>C
(GRCh38)19:52212729C>T
(Homo sapiens)Allele/Variant
Source: rs1057519946
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212729C>T
(GRCh38)19:52212730G>A
(Homo sapiens)Allele/Variant
Source: rs1057519947
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212730G>A
(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)19:52205951T>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)19:52213019A>T
(Homo sapiens)Allele/Variant
Source: rs2089687182
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213019A>T
(GRCh38)19:52213076G>A
(Homo sapiens)Allele/Variant
Source: rs863225094
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213076G>A