Version: 8.1.0
Date: Fri Apr 18 2025
240 results for plap
Allele/Variant Molecular Consequence: synonymous variant

(GRCh38)9:26920272A>T

(Homo sapiens)
Allele/Variant
Source: rs766216764
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920272A>T
Gene Synonyms: PLAP

(GRCh38)9:26905965T>C

(Homo sapiens)
Allele/Variant
Source: rs1385484105
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905965T>C
Gene Synonyms: PLAP

(GRCh38)9:26928198G>A

(Homo sapiens)
Allele/Variant
Source: rs566272935
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928198G>A
Gene Synonyms: PLAP

(GRCh38)9:26913898G>A

(Homo sapiens)
Allele/Variant
Source: rs370264645
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913898G>A
Gene Synonyms: PLAP

(GRCh38)9:26919500G>A

(Homo sapiens)
Allele/Variant
Source: rs2131379778
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919500G>A
Gene Synonyms: PLAP

(GRCh38)9:26920239T>C

(Homo sapiens)
Allele/Variant
Source: rs962382467
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920239T>C
Gene Synonyms: PLAP

(GRCh38)9:26905592A>G

(Homo sapiens)
Allele/Variant
Source: rs781766738
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905592A>G
Gene Synonyms: PLAP

(GRCh38)9:26905977C>T

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26905977C>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905977C>T
Gene Synonyms: PLAP

(GRCh38)9:26906057A>C

(Homo sapiens)
Allele/Variant
Source: rs573201333
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_lost, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26906057A>C
Gene Synonyms: PLAP

(GRCh38)9:26928197C>T

(Homo sapiens)
Allele/Variant
Source: rs771441156
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928197C>T
Gene Synonyms: PLAP

(GRCh38)9:26905544A>G

(Homo sapiens)
Allele/Variant
Source: rs2131360575
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905544A>G
Gene Synonyms: PLAP

(GRCh38)9:26928395T>C

(Homo sapiens)
Allele/Variant
Source: rs1251664115
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928395T>C
Gene Synonyms: PLAP

(GRCh38)9:26946947G>C

(Homo sapiens)
Allele/Variant
Source: rs368369595
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26946947G>C
Gene Synonyms: PLAP

(GRCh38)9:26935098G>T

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26935098G>T
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935098G>T
Gene Synonyms: PLAP

(GRCh38)9:26935114G>C

(Homo sapiens)
Allele/Variant
Source: rs899332673
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935114G>C
Gene Synonyms: PLAP

(GRCh38)9:26910393A>G

(Homo sapiens)
Allele/Variant
Source: rs543116052
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910393A>G
Gene Synonyms: PLAP

(GRCh38)9:26913938C>A

(Homo sapiens)
Allele/Variant
Source: rs150012469
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913938C>A
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)9:26919452G>A

(Homo sapiens)
Allele/Variant
Source: rs1824680953
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919452G>A
Gene Synonyms: PLAP

(GRCh38)9:26928120C>T

(Homo sapiens)
Allele/Variant
Source: rs1206910244
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928120C>T
Gene Synonyms: PLAP

(GRCh38)9:26910425G>A

(Homo sapiens)
Allele/Variant
Source: rs1241511703
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910425G>A
Gene Synonyms: PLAP

(GRCh38)9:26913885A>G

(Homo sapiens)
Allele/Variant
Source: rs1438160394
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913885A>G
Gene Synonyms: PLAP

(GRCh38)9:26913897C>T

(Homo sapiens)
Allele/Variant
Source: rs139288553
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913897C>T
Gene Synonyms: PLAP

(GRCh38)9:26923236G>A

(Homo sapiens)
Allele/Variant
Source: rs75789871
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923236G>A
Gene Synonyms: PLAP

(GRCh38)9:26923296A>G

(Homo sapiens)
Allele/Variant
Source: rs1379209247
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923296A>G
Gene Synonyms: PLAP

(GRCh38)9:26923308T>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26923308T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923308T>G
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)9:26946935C>T

(Homo sapiens)
Allele/Variant
Source: rs965904192
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26946935C>T
Gene Synonyms: PLAP

(GRCh38)9:26946947G>A

(Homo sapiens)
Allele/Variant
Source: rs368369595
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26946947G>A
Gene Synonyms: PLAP

(GRCh38)9:26920368C>T

(Homo sapiens)
Allele/Variant
Source: rs773630798
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920368C>T
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)9:26907877G>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)9:26913934A>G

(Homo sapiens)
Allele/Variant
Source: rs778419345
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913934A>G
Gene Synonyms: PLAP

(GRCh38)9:26923314T>C

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26923314T>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923314T>C
Gene Synonyms: PLAP

(GRCh38)9:26925827C>T

(Homo sapiens)
Allele/Variant
Source: rs1352823433
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26925827C>T
Gene Synonyms: PLAP

(GRCh38)9:26926542C>T

(Homo sapiens)
Allele/Variant
Source: rs957863558
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26926542C>T
Gene Synonyms: PLAP

(GRCh38)9:26935048A>G

(Homo sapiens)
Allele/Variant
Source: rs199968569
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935048A>G
Gene Synonyms: PLAP

(GRCh38)9:26913903T>C

(Homo sapiens)
Allele/Variant
Source: rs1824471495
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26913903T>C
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)9:26907827T>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)9:26919461G>A

(Homo sapiens)
Allele/Variant
Source: rs200655405
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919461G>A
Gene Synonyms: PLAP

(GRCh38)9:26923305T>C

(Homo sapiens)
Allele/Variant
Source: rs370728877
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923305T>C
Gene Synonyms: PLAP

(GRCh38)9:26910436T>C

(Homo sapiens)
Allele/Variant
Source: rs150830660
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910436T>C
Gene Synonyms: PLAP

(GRCh38)9:26919498T>C

(Homo sapiens)
Allele/Variant
Source: rs1381447481
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919498T>C
Gene Synonyms: PLAP

(GRCh38)9:26926559C>A

(Homo sapiens)
Allele/Variant
Source: rs371109788
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26926559C>A
Gene Synonyms: PLAP

(GRCh38)9:26935034G>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26935034G>A
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935034G>A
Gene Synonyms: PLAP

(GRCh38)9:26947004G>C

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26947004G>C
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26947004G>C
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)9:26920275T>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26920275T>A
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920275T>A
Gene Synonyms: PLAP

(GRCh38)9:26905968A>G

(Homo sapiens)
Allele/Variant
Source: rs1255165207
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905968A>G
Gene Synonyms: PLAP