Version: 8.0.0
Date: Tue Jan 28 2025
440 results for pp2aa

(GRCh38)19:52211439C>G

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52211439C>G
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)19:52211439C>G
Gene Synonyms: PP2AA

(GRCh38)19:52211459G>A

(Homo sapiens)
Allele/Variant
Source: rs111525410
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)19:52211459G>A
Gene Synonyms: PP2AA

(GRCh38)19:52216035G>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52216035G>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216035G>C
Gene Synonyms: PP2AA

(GRCh38)19:52216582C>T

(Homo sapiens)
Allele/Variant
Source: rs1334151690
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)19:52216582C>T
Gene Synonyms: PP2AA

(GRCh38)19:52213040C>G

(Homo sapiens)
Allele/Variant
Source: rs2122338423
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213040C>G
Gene Synonyms: PP2AA

(GRCh38)19:52213054G>T

(Homo sapiens)
Allele/Variant
Source: rs777150923
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213054G>T
Gene Synonyms: PP2AA

(GRCh38)19:52221085C>T

(Homo sapiens)
Allele/Variant
Source: rs187141962
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)19:52221085C>T
Gene Synonyms: PP2AA

(GRCh38)19:52221096A>G

(Homo sapiens)
Allele/Variant
Source: rs1285312270
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)19:52221096A>G
Gene Synonyms: PP2AA

(GRCh38)19:52221102T>C

(Homo sapiens)
Allele/Variant
Source: rs1978897316
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)19:52221102T>C
Gene Synonyms: PP2AA

(GRCh38)19:52219852G>A

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52219852G>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)19:52219852G>A
Gene Synonyms: PP2AA

(GRCh38)19:52222083A>G

(Homo sapiens)
Allele/Variant
Source: rs979543577
Genes: MIR6801 (Hsa), 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)19:52222083A>G
Gene Synonyms: PP2AA

(GRCh38)19:52212997G>T

(Homo sapiens)
Allele/Variant
Source: rs769334090
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212997G>T
Gene Synonyms: PP2AA

(GRCh38)19:52216033C>A

(Homo sapiens)
Allele/Variant
Source: rs775654171
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216033C>A
Gene Synonyms: PP2AA

(GRCh38)19:52216594T>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52216594T>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)19:52216594T>C
Gene Synonyms: PP2AA

(GRCh38)19:52216631T>C

(Homo sapiens)
Allele/Variant
Source: rs1256454080
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)19:52216631T>C
Gene Synonyms: PP2AA

(GRCh38)19:52216639C>A

(Homo sapiens)
Allele/Variant
Source: rs1179597654
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)19:52216639C>A
Gene Synonyms: PP2AA

(GRCh38)19:52222133C>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52222133C>T
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)19:52222133C>T
Gene Synonyms: PP2AA

(GRCh38)19:52222160G>A

(Homo sapiens)
Allele/Variant
Source: rs758740333
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)19:52222160G>A
Gene Synonyms: PP2AA

(GRCh38)19:52222175C>T

(Homo sapiens)
Allele/Variant
Source: rs1194775389
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)19:52222175C>T
Gene Synonyms: PP2AA

(GRCh38)19:52219820C>T

(Homo sapiens)
Allele/Variant
Source: rs759316091
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)19:52219820C>T
Gene Synonyms: PP2AA

(GRCh38)19:52221051A>G

(Homo sapiens)
Allele/Variant
Source: rs141690261
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)19:52221051A>G
Gene Synonyms: PP2AA

(GRCh38)19:52212827C>T

(Homo sapiens)
Allele/Variant
Source: rs150469675
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212827C>T
Gene Synonyms: PP2AA

(GRCh38)19:52212957C>G

(Homo sapiens)
Allele/Variant
Source: rs1371810473
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)19:52212957C>G
Gene Synonyms: PP2AA

(GRCh38)19:52212981G>A

(Homo sapiens)
Allele/Variant
Source: rs11537697
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212981G>A
Gene Synonyms: PP2AA

(GRCh38)19:52225726G>C

(Homo sapiens)
Allele/Variant
Source: rs767632211
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52225726G>C
Gene Synonyms: PP2AA

(GRCh38)19:52190236C>G

(Homo sapiens)
Allele/Variant
Source: rs575654670
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)19:52190236C>G
Gene Synonyms: PP2AA

(GRCh38)19:52216092G>A

(Homo sapiens)
Allele/Variant
Source: rs1223573387
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216092G>A
Gene Synonyms: PP2AA

(GRCh38)19:52220183C>T

(Homo sapiens)
Allele/Variant
Source: rs77987409
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)19:52220183C>T
Gene Synonyms: PP2AA

(GRCh38)19:52220221C>T

(Homo sapiens)
Allele/Variant
Source: rs1298281898
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)19:52220221C>T
Gene Synonyms: PP2AA

(GRCh38)19:52221150C>T

(Homo sapiens)
Allele/Variant
Source: rs769292996
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221150C>T
Gene Synonyms: PP2AA

(GRCh38)19:52190256T>G

(Homo sapiens)
Allele/Variant
Source: rs114390941
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)19:52190256T>G
Gene Synonyms: PP2AA

(GRCh38)19:52216512C>T

(Homo sapiens)
Allele/Variant
Source: rs1978584320
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52216512C>T
Gene Synonyms: PP2AA

(GRCh38)19:52225714C>T

(Homo sapiens)
Allele/Variant
Source: rs572638720
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)19:52225714C>T
Gene Synonyms: PP2AA

(GRCh38)19:52211415C>T

(Homo sapiens)
Allele/Variant
Source: rs774301300
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)19:52211415C>T
Gene Synonyms: PP2AA

(GRCh38)19:52215877C>T

(Homo sapiens)
Allele/Variant
Source: rs1397821742
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215877C>T
Gene Synonyms: PP2AA

(GRCh38)19:52216641T>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52216641T>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)19:52216641T>C
Gene Synonyms: PP2AA

(GRCh38)19:52219702A>T

(Homo sapiens)
Allele/Variant
Source: rs2122360173
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)19:52219702A>T
Gene Synonyms: PP2AA

(GRCh38)19:52221024T>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52221024T>C
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)19:52221024T>C
Gene Synonyms: PP2AA

(GRCh38)19:52212735G>A

(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>A
Gene Synonyms: PP2AA

(GRCh38)19:52201991T>C

(Homo sapiens)
Allele/Variant
Source: rs951343132
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)19:52201991T>C
Gene Synonyms: PP2AA

(GRCh38)19:52202045G>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52202045G>C
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>C
Gene Synonyms: PP2AA

(GRCh38)19:52212962T>G

(Homo sapiens)
Allele/Variant
Source: rs2122337425
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212962T>G
Gene Synonyms: PP2AA

(GRCh38)19:52215813C>G

(Homo sapiens)
Allele/Variant
Source: rs1568595903
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215813C>G
Gene Synonyms: PP2AA

(GRCh38)19:52215813C>T

(Homo sapiens)
Allele/Variant
Source: rs1568595903
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215813C>T
Gene Synonyms: PP2AA

(GRCh38)19:52215823C>G

(Homo sapiens)
Allele/Variant
Source: rs925061835
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215823C>G
Gene Synonyms: PP2AA

(GRCh38)19:52215872G>A

(Homo sapiens)
Allele/Variant
Source: rs771769470
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>A
Gene Synonyms: PP2AA

(GRCh38)19:52190169G>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52190169G>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)19:52190169G>T
Gene Synonyms: PP2AA

(GRCh38)19:52211466C>T

(Homo sapiens)
Allele/Variant
Source: rs11537695
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)19:52211466C>T
Gene Synonyms: PP2AA

(GRCh38)19:52211472T>C

(Homo sapiens)
Allele/Variant
Source: rs770017081
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)19:52211472T>C
Gene Synonyms: PP2AA

(GRCh38)19:52222152G>A

(Homo sapiens)
Allele/Variant
Source: rs147064842
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)19:52222152G>A
Gene Synonyms: PP2AA