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

(GRCh38)19:52222160G>T

(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>T
Gene Synonyms: PP2AA

(GRCh38)19:52219814C>T

(Homo sapiens)
Allele/Variant
Source: rs770861676
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)19:52219814C>T
Gene Synonyms: PP2AA

(GRCh38)19:52221039A>G

(Homo sapiens)
Allele/Variant
Source: rs760153767
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)19:52221039A>G
Gene Synonyms: PP2AA

(GRCh38)19:52212718C>T

(Homo sapiens)
Allele/Variant
Source: rs786205228
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)19:52212718C>T
Gene Synonyms: PP2AA

(GRCh38)19:52212744A>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52212744A>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212744A>C
Gene Synonyms: PP2AA

(GRCh38)19:52213048C>T

(Homo sapiens)
Allele/Variant
Source: rs2089687609
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213048C>T
Gene Synonyms: PP2AA

(GRCh38)19:52215835G>T

(Homo sapiens)
Allele/Variant
Source: rs2122348542
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215835G>T
Gene Synonyms: PP2AA

(GRCh38)19:52225754C>T

(Homo sapiens)
Allele/Variant
Source: rs756971999
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)19:52225754C>T
Gene Synonyms: PP2AA

(GRCh38)19:52190126G>A

(Homo sapiens)
Allele/Variant
Source: rs2122267687
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)19:52190126G>A
Gene Synonyms: PP2AA

(GRCh38)19:52190136G>T

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52190136G>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)19:52190136G>T
Gene Synonyms: PP2AA

(GRCh38)19:52212990G>C

(Homo sapiens)
Allele/Variant
Source: rs1285802488
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212990G>C
Gene Synonyms: PP2AA

(GRCh38)19:52215880C>T

(Homo sapiens)
Allele/Variant
Source: rs371666912
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52215880C>T
Gene Synonyms: PP2AA

(GRCh38)19:52213000C>G

(Homo sapiens)
Allele/Variant
Source: rs2122337914
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213000C>G
Gene Synonyms: PP2AA

(GRCh38)19:52216607A>G

(Homo sapiens)
Allele/Variant
Source: rs1978589380
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)19:52216607A>G
Gene Synonyms: PP2AA

(GRCh38)19:52219727G>A

(Homo sapiens)
Allele/Variant
Source: rs2122360256
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)19:52219727G>A
Gene Synonyms: PP2AA

(GRCh38)19:52219762G>A

(Homo sapiens)
Allele/Variant
Source: rs748379874
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)19:52219762G>A
Gene Synonyms: PP2AA

(GRCh38)19:52212750G>T

(Homo sapiens)
Allele/Variant
Source: rs2122335090
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212750G>T
Gene Synonyms: PP2AA

(GRCh38)19:52212752G>A

(Homo sapiens)
Allele/Variant
Source: rs760464308
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212752G>A
Gene Synonyms: PP2AA

(GRCh38)19:52212753G>A

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52212753G>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)19:52212753G>A
Gene Synonyms: PP2AA

(GRCh38)19:52205950C>G

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52205950C>G
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)19:52205950C>G
Gene Synonyms: PP2AA

(GRCh38)19:52205998C>T

(Homo sapiens)
Allele/Variant
Source: rs774799372
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)19:52205998C>T
Gene Synonyms: PP2AA

(GRCh38)19:52212783G>A

(Homo sapiens)
Allele/Variant
Source: rs749905469
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212783G>A
Gene Synonyms: PP2AA

(GRCh38)19:52212670C>T

(Homo sapiens)
Allele/Variant
Source: rs753055903
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)19:52212670C>T
Gene Synonyms: PP2AA

(GRCh38)19:52221153G>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52221153G>C
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52221153G>C
Gene Synonyms: PP2AA

(GRCh38)19:52212951C>G

(Homo sapiens)
Allele/Variant
Source: rs765444755
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52212951C>G
Gene Synonyms: PP2AA

(GRCh38)19:52219846C>T

(Homo sapiens)
Allele/Variant
Source: rs771749848
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)19:52219846C>T
Gene Synonyms: PP2AA

(GRCh38)19:52211332A>G

(Homo sapiens)
Allele/Variant
Source: rs965521747
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)19:52211332A>G
Gene Synonyms: PP2AA

(GRCh38)19:52221116A>G

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52221116A>G
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)19:52221116A>G
Gene Synonyms: PP2AA

(GRCh38)19:52213125G>A

(Homo sapiens)
Allele/Variant
Source: rs749010282
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213125G>A
Gene Synonyms: PP2AA

(GRCh38)19:52215759C>T

(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>T
Gene Synonyms: PP2AA

(GRCh38)19:52219834T>C

(Homo sapiens)
Allele/Variant
Source: rs1200174357
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)19:52219834T>C
Gene Synonyms: PP2AA

(GRCh38)19:52220975G>C

(Homo sapiens)
Allele/Variant
Source: rs1978886421
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)19:52220975G>C
Gene Synonyms: PP2AA

(GRCh38)19:52225828G>A

(Homo sapiens)
Allele/Variant
Source: rs772093250
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)19:52225828G>A
Gene Synonyms: PP2AA

(GRCh38)19:52211419C>T

(Homo sapiens)
Allele/Variant
Source: rs2122329969
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)19:52211419C>T
Gene Synonyms: PP2AA

(GRCh38)19:52190179G>A

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.52190179G>A
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52190179G>A
Gene Synonyms: PP2AA

(GRCh38)19:52213121G>A

(Homo sapiens)
Allele/Variant
Source: rs370859682
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52213121G>A
Gene Synonyms: PP2AA

(GRCh38)19:52215759C>G

(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>G
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(GRCh38)19:52202046G>A

(Homo sapiens)
Allele/Variant
Source: rs200369713
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202046G>A
Gene Synonyms: PP2AA

(GRCh38)19:52202051C>A

(Homo sapiens)
Allele/Variant
Source: rs1421549263
Genes: PPP2R1A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:52202051C>A
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(GRCh38)19:52206025A>C

(Homo sapiens)
Allele/Variant
Source: rs559725266
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>C
Gene Synonyms: PP2AA

(GRCh38)19:52206052C>T

(Homo sapiens)
Allele/Variant
Source: rs144146832
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)19:52206052C>T
Gene Synonyms: PP2AA

(GRCh38)19:52201928C>A

(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>A
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA

(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
Gene Synonyms: PP2AA