Version: 8.1.0
Date: Fri Apr 18 2025
2,715 results for 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)9:26935157A>C

(Homo sapiens)
Allele/Variant
Source: rs757313107
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26935157A>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)9:26910382T>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26910382T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26910382T>G
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)9:26913871G>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)9:26913885A>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)9:26917078A>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)9:26923236G>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)9:26923253T>C

(Homo sapiens)
Allele/Variant
Source: rs2131386997
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923253T>C
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)9:26907841A>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)9:26913934A>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)9:26907815T>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)9:26925827C>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)9:26926444A>G

(Homo sapiens)
Allele/Variant
Source: rs1336797898
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26926444A>G
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)9:26920220G>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)9:26920226C>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26920226C>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920226C>G
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)9:26920300A>T

(Homo sapiens)
Allele/Variant
Source: rs2131381287
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920300A>T
Gene Synonyms: PLAP

(GRCh38)9:26919460T>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26919460T>A
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919460T>A
Gene Synonyms: PLAP

(GRCh38)9:26919468T>C

(Homo sapiens)
Allele/Variant
Source: rs1164031152
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26919468T>C
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)9:26923315T>A

(Homo sapiens)
Allele/Variant
Source: rs140755075
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923315T>A
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)9:26905635T>C

(Homo sapiens)
Allele/Variant
Source: rs78886918
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905635T>C
Gene Synonyms: PLAP

(GRCh38)9:26905638C>T

(Homo sapiens)
Allele/Variant
Source: rs1206597535
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905638C>T
Gene Synonyms: PLAP

(GRCh38)9:26905897C>T

(Homo sapiens)
Allele/Variant
Source: rs137995823
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905897C>T
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)9:26907822G>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)9:26928142C>G

(Homo sapiens)
Allele/Variant
Source: rs1263525837
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26928142C>G
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)9:26928293A>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)9:26919461G>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)9:26923220T>G

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26923220T>G
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923220T>G
Gene Synonyms: PLAP

(GRCh38)9:26923250C>A

(Homo sapiens)
Allele/Variant
Source: rs149976633
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923250C>A
Gene Synonyms: PLAP

(GRCh38)9:26923262G>A

(Homo sapiens)
Allele/Variant
Source: rs753300259
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26923262G>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)9:26905811C>A

(Homo sapiens)
Allele/Variant
Source: rs1049445907
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26905811C>A
Gene Synonyms: PLAP