Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PPP2R1A (Hsa) Molecular Consequence: non coding transcript variant
(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)19:52211389C>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)19:52222127T>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)19:52212721T>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)19:52213019A>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)19:52211274G>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)19:52222168G>A
(Homo sapiens)Allele/Variant
Source: rs766471656
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222168G>A
(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)19:52212983C>T
(Homo sapiens)Allele/Variant
Source: rs945817997
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212983C>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)19:52215872G>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52215872G>T
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215872G>T
(GRCh38)19:52212786A>C
(Homo sapiens)Allele/Variant
Source: rs759982626
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212786A>C
(GRCh38)19:52211366C>T
(Homo sapiens)Allele/Variant
Source: rs527266620
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)19:52211366C>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)19:52225802C>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)19:52211310G>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)19:52213056C>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)19:52213078G>A
(Homo sapiens)Allele/Variant
Source: rs2089688265
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213078G>A
(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)19:52216042G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52216042G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216042G>A
(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)19:52212735G>T
(Homo sapiens)Allele/Variant
Source: rs1348762266
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212735G>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)19:52225719C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52225719C>G
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225719C>G
(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
(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)19:52211306A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.52211306A>G
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)19:52211306A>G
(GRCh38)19:52211437C>G
(Homo sapiens)Allele/Variant
Source: rs1369744426
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)19:52211437C>G
(GRCh38)19:52222130C>G
(Homo sapiens)Allele/Variant
Source: rs2122369413
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52222130C>G
(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)19:52212721T>G
(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>G
(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