Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Allele/Variant Molecular Consequence: intron variant
(GRCh38)9:26920220G>A
(Homo sapiens)Allele/Variant
Source: rs201196073
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920220G>A
Gene Synonyms: PLAP
(GRCh38)9:26923174T>C
(Homo sapiens)Allele/Variant
Source: rs1446485952
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923174T>C
Gene Synonyms: PLAP
(GRCh38)9:26907822G>C
(Homo sapiens)Allele/Variant
Source: rs770300192
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907822G>C
Gene Synonyms: PLAP
(GRCh38)9:26926578A>G
(Homo sapiens)Allele/Variant
Source: rs771248758
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26926578A>G
Gene Synonyms: PLAP
(GRCh38)9:26928293A>G
(Homo sapiens)Allele/Variant
Source: rs376780468
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928293A>G
Gene Synonyms: PLAP
(GRCh38)9:26907905C>T
(Homo sapiens)Allele/Variant
Source: rs2131363846
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907905C>T
Gene Synonyms: PLAP
(GRCh38)9:26908012C>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26908012C>A
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26908012C>A
Gene Synonyms: PLAP
(GRCh38)9:26910334T>C
(Homo sapiens)Allele/Variant
Source: rs1164105744
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910334T>C
Gene Synonyms: PLAP
(GRCh38)9:26913867A>G
(Homo sapiens)Allele/Variant
Source: rs778225031
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913867A>G
Gene Synonyms: PLAP
(GRCh38)9:26917081C>G
(Homo sapiens)Allele/Variant
Source: rs538989439
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917081C>G
Gene Synonyms: PLAP
(GRCh38)9:26923359A>C
(Homo sapiens)Allele/Variant
Source: rs1824835966
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923359A>C
Gene Synonyms: PLAP
(GRCh38)9:26923361T>G
(Homo sapiens)Allele/Variant
Source: rs529320124
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923361T>G
Gene Synonyms: PLAP
(GRCh38)9:26923367G>T
(Homo sapiens)Allele/Variant
Source: rs1824836492
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923367G>T
Gene Synonyms: PLAP
(GRCh38)9:26906093G>T
(Homo sapiens)Allele/Variant
Source: rs750356765
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26906093G>T
Gene Synonyms: PLAP
(GRCh38)9:26917089C>T
(Homo sapiens)Allele/Variant
Source: rs778992139
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917089C>T
Gene Synonyms: PLAP
(GRCh38)9:26907891C>G
(Homo sapiens)Allele/Variant
Source: rs2131363823
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907891C>G
Gene Synonyms: PLAP
(GRCh38)9:26913954T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26913954T>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913954T>C
Gene Synonyms: PLAP
(GRCh38)9:26917146C>T
(Homo sapiens)Allele/Variant
Source: rs201133026
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917146C>T
Gene Synonyms: PLAP
(GRCh38)9:26923158A>G
(Homo sapiens)Allele/Variant
Source: rs895528320
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923158A>G
Gene Synonyms: PLAP
(GRCh38)9:26926580T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26926580T>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26926580T>C
Gene Synonyms: PLAP
(GRCh38)9:26913871G>T
(Homo sapiens)Allele/Variant
Source: rs747382266
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913871G>T
Gene Synonyms: PLAP
(GRCh38)9:26917078A>G
(Homo sapiens)Allele/Variant
Source: rs141342759
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917078A>G
Gene Synonyms: PLAP
(GRCh38)9:26928233T>C
(Homo sapiens)Allele/Variant
Source: rs960695016
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928233T>C
Gene Synonyms: PLAP
(GRCh38)9:26935200G>A
(Homo sapiens)Allele/Variant
Source: rs868428372
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935200G>A
Gene Synonyms: PLAP
(GRCh38)9:26925809A>T
(Homo sapiens)Allele/Variant
Source: rs566459503
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925809A>T
Gene Synonyms: PLAP
(GRCh38)9:26925813G>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26925813G>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925813G>C
Gene Synonyms: PLAP
(GRCh38)9:26919542T>C
(Homo sapiens)Allele/Variant
Source: rs10120313
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919542T>C
Gene Synonyms: PLAP
(GRCh38)9:26917127T>C
(Homo sapiens)Allele/Variant
Source: rs776400772
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917127T>C
Gene Synonyms: PLAP
(GRCh38)9:26917137C>T
(Homo sapiens)Allele/Variant
Source: rs764801859
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917137C>T
Gene Synonyms: PLAP
(GRCh38)9:26907933G>A
(Homo sapiens)Allele/Variant
Source: rs148248479
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907933G>A
Gene Synonyms: PLAP
(GRCh38)9:26907841A>G
(Homo sapiens)Allele/Variant
Source: rs1227890958
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907841A>G
Gene Synonyms: PLAP
(GRCh38)9:26907856C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26907856C>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907856C>T
Gene Synonyms: PLAP
(GRCh38)9:26907877G>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26907877G>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907877G>C
Gene Synonyms: PLAP
(GRCh38)9:26907906A>G
(Homo sapiens)Allele/Variant
Source: rs1375805046
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907906A>G
Gene Synonyms: PLAP
(GRCh38)9:26907815T>C
(Homo sapiens)Allele/Variant
Source: rs1207928638
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907815T>C
Gene Synonyms: PLAP
(GRCh38)9:26910325T>G
(Homo sapiens)Allele/Variant
Source: rs376697127
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910325T>G
Gene Synonyms: PLAP
(GRCh38)9:26917140A>C
(Homo sapiens)Allele/Variant
Source: rs768076485
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917140A>C
Gene Synonyms: PLAP
(GRCh38)9:26919293T>C
(Homo sapiens)Allele/Variant
Source: rs370013195
Genes: PLAA (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)9:26919293T>C
Gene Synonyms: PLAP
(GRCh38)9:26907827T>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26907827T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, stop_lost, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907827T>G
Gene Synonyms: PLAP
(GRCh38)9:26910326A>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26910326A>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910326A>G
Gene Synonyms: PLAP
(GRCh38)9:26917091T>A
(Homo sapiens)Allele/Variant
Source: rs189073379
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917091T>A
Gene Synonyms: PLAP
(GRCh38)9:26925975T>A
(Homo sapiens)Allele/Variant
Source: rs541931169
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925975T>A
Gene Synonyms: PLAP
(GRCh38)9:26925977T>C
(Homo sapiens)Allele/Variant
Source: rs372889383
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925977T>C
Gene Synonyms: PLAP
(GRCh38)9:26928301A>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26928301A>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928301A>T
Gene Synonyms: PLAP
(GRCh38)9:26946892C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.26946892C>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26946892C>T
Gene Synonyms: PLAP
(GRCh38)9:26917125G>A
(Homo sapiens)Allele/Variant
Source: rs1824588299
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917125G>A
Gene Synonyms: PLAP
(GRCh38)9:26923362A>C
(Homo sapiens)Allele/Variant
Source: rs753208493
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923362A>C
Gene Synonyms: PLAP
(GRCh38)9:26925806T>C
(Homo sapiens)Allele/Variant
Source: rs183448864
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925806T>C
Gene Synonyms: PLAP
(GRCh38)9:26907987C>G
(Homo sapiens)Allele/Variant
Source: rs374665187
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26907987C>G
Gene Synonyms: PLAP
(GRCh38)9:26919305C>T
(Homo sapiens)Allele/Variant
Source: rs1039511340
Genes: PLAA (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)9:26919305C>T
Gene Synonyms: PLAP