Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PPP2R1A (Hsa) Molecular Consequence: synonymous 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)19:52222127T>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)19:52201979C>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)19:52213077C>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)19:52219852G>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)19:52219804C>T
(Homo sapiens)Allele/Variant
Source: rs139139629
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)19:52219804C>T
(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)19:52215829C>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)19:52215871C>T
(Homo sapiens)Allele/Variant
Source: rs745513453
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215871C>T
(GRCh38)19:52225749A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52225749A>G
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)19:52225749A>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)19:52211484A>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)19:52221106C>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)19:52212984G>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)19:52212957C>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)19:52212984G>A
(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>A
(GRCh38)19:52216549C>T
(Homo sapiens)Allele/Variant
Source: rs1032440574
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216549C>T
(GRCh38)19:52222158G>A
(Homo sapiens)Allele/Variant
Source: rs748399975
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)19:52222158G>A
(GRCh38)19:52222176G>A
(Homo sapiens)Allele/Variant
Source: rs141304480
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)19:52222176G>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)19:52213056C>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)19:52216020C>T
(Homo sapiens)Allele/Variant
Source: rs771332782
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216020C>T
(GRCh38)19:52216597C>G
(Homo sapiens)Allele/Variant
Source: rs1315395253
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)19:52216597C>G
(GRCh38)19:52216618C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216618C>T
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)19:52216618C>T
(GRCh38)19:52222191C>T
(Homo sapiens)Allele/Variant
Source: rs1978980122
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)19:52222191C>T
(GRCh38)19:52202027C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52202027C>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202027C>T
(GRCh38)19:52212975G>A
(Homo sapiens)Allele/Variant
Source: rs371185672
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212975G>A
(GRCh38)19:52190132C>T
(Homo sapiens)Allele/Variant
Source: rs768487870
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)19:52190132C>T
(GRCh38)19:52222110G>A
(Homo sapiens)Allele/Variant
Source: rs777348773
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222110G>A
(GRCh38)19:52219738C>T
(Homo sapiens)Allele/Variant
Source: rs143253734
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)19:52219738C>T
(GRCh38)19:52222136A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52222136A>G
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)19:52222136A>G
(GRCh38)19:52222151C>T
(Homo sapiens)Allele/Variant
Source: rs747537922
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)19:52222151C>T
(GRCh38)19:52215859C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52215859C>G
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215859C>G
(GRCh38)19:52211340C>T
(Homo sapiens)Allele/Variant
Source: rs752257198
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)19:52211340C>T
(GRCh38)19:52211481G>A
(Homo sapiens)Allele/Variant
Source: rs200540971
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)19:52211481G>A
(GRCh38)19:52212996C>T
(Homo sapiens)Allele/Variant
Source: rs149134744
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212996C>T
(GRCh38)19:52205994G>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52205994G>C
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)19:52205994G>C