Version: 8.0.0
Date: Tue Jan 28 2025
439 results
Allele/Variant Genes: PPP2R1A (Hsa)

(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)19:52190108C>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

(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

(GRCh38)19:52225709C>T

(Homo sapiens)
Allele/Variant
Source: rs2122381571
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)19:52225709C>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)19:52219876G>A

(Homo sapiens)
Allele/Variant
Source: rs1042762884
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52219876G>A

(GRCh38)19:52220963C>G

(Homo sapiens)
Allele/Variant
Source: rs8100816
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52220963C>G

(GRCh38)19:52225827G>A

(Homo sapiens)
Allele/Variant
Source: rs549622974
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)19:52225827G>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)19:52211306A>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)19:52190162T>A

(Homo sapiens)
Allele/Variant
Source: rs2122267837
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)19:52190162T>A

(GRCh38)19:52200275G>A

(Homo sapiens)
Allele/Variant
Source: rs189657964
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52200275G>A

(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)19:52222110G>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)19:52222130C>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

(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)19:52212715C>T

(Homo sapiens)
Allele/Variant
Source: rs2122334581
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)19:52212715C>T

(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

(GRCh38)19:52225726G>A

(Homo sapiens)
Allele/Variant
Source: rs767632211
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)19:52225726G>A

(GRCh38)19:52212823C>G

(Homo sapiens)
Allele/Variant
Source: rs1284984038
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212823C>G

(GRCh38)19:52215842A>T

(Homo sapiens)
Allele/Variant
Source: rs753529647
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215842A>T

(GRCh38)19:52225785A>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52225785A>C
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)19:52225785A>C

(GRCh38)19:52216633G>A

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52216633G>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)19:52216633G>A

(GRCh38)19:52201961C>G

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52201961C>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)19:52201961C>G

(GRCh38)19:52206000G>T

(Homo sapiens)
Allele/Variant
Source: rs1477794653
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)19:52206000G>T

(GRCh38)19:52215787A>G

(Homo sapiens)
Allele/Variant
Source: rs969553207
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215787A>G

(GRCh38)19:52215797C>T

(Homo sapiens)
Allele/Variant
Source: rs777655260
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215797C>T

(GRCh38)19:52221108G>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52221108G>T
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)19:52221108G>T

(GRCh38)19:52216554A>G

(Homo sapiens)
Allele/Variant
Source: rs1978587530
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216554A>G

(GRCh38)19:52216621C>T

(Homo sapiens)
Allele/Variant
Source: rs370489148
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)19:52216621C>T