1,815 results for plap
Allele/Variant Molecular Consequence: non coding transcript 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)9:26920226C>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)9:26917081C>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)9:26917091T>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)9:26919305C>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

(GRCh38)9:26917171C>T

(Homo sapiens)
Allele/Variant
Source: rs1259209891
Genes: PLAA (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)9:26917171C>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)9:26917172A>G

(Homo sapiens)
Allele/Variant
Source: rs972207702
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917172A>G
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)9:26919542T>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)9:26919291A>T

(Homo sapiens)
Allele/Variant
Source: rs527667422
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)9:26919291A>T
Gene Synonyms: PLAP

(GRCh38)9:26920216A>G

(Homo sapiens)
Allele/Variant
Source: rs769128926
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920216A>G
Gene Synonyms: PLAP

(GRCh38)9:26920219C>G

(Homo sapiens)
Allele/Variant
Source: rs548381785
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)9:26920219C>G
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)9:26919290C>A

(Homo sapiens)
Allele/Variant
Source: rs1824675315
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)9:26919290C>A
Gene Synonyms: PLAP

(GRCh38)9:26919296A>G

(Homo sapiens)
Allele/Variant
Source: rs1235467407
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)9:26919296A>G
Gene Synonyms: PLAP

(GRCh38)9:26920207G>C

(Homo sapiens)
Allele/Variant
Source: rs201598009
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26920207G>C
Gene Synonyms: PLAP

(GRCh38)9:26917080T>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.26917080T>A
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917080T>A
Gene Synonyms: PLAP

(GRCh38)9:26917087T>C

(Homo sapiens)
Allele/Variant
Source: rs557098359
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917087T>C
Gene Synonyms: PLAP

(GRCh38)9:26920219C>T

(Homo sapiens)
Allele/Variant
Source: rs548381785
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)9:26920219C>T
Gene Synonyms: PLAP

(GRCh38)9:26917180T>C

(Homo sapiens)
Allele/Variant
Source: rs201496988
Genes: PLAA (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:26917180T>C
Gene Synonyms: PLAP

Allele/Variant
Source: rs45896883
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105762648C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs230554613
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105762649G>A
Gene Synonyms: Plap

Allele/Variant
Source: rs49850305
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105762802C>A
Gene Synonyms: Plap

Allele/Variant
Source: rs248588537
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105762822C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs261435909
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105763317G>T
Gene Synonyms: Plap

Allele/Variant
Source: rs586069522
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105757250A>G
Gene Synonyms: Plap

Allele/Variant
Source: rs217315277
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105757867C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs258896649
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105751815C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs47114884
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105758668G>A
Gene Synonyms: Plap

Allele/Variant
Source: rs233824126
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105759207A>G
Gene Synonyms: Plap

Allele/Variant
Source: rs252483218
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105751460T>A
Gene Synonyms: Plap

Allele/Variant
Source: rs256382735
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105751843G>A
Gene Synonyms: Plap

Allele/Variant
Source: rs241147808
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105760613G>A
Gene Synonyms: Plap

Allele/Variant
Source: rs216998169
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105760799C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs49272275
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105765287T>A
Gene Synonyms: Plap

Allele/Variant
Source: rs235518923
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105765476A>G
Gene Synonyms: Plap

Allele/Variant
Source: rs245539098
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105764430T>G
Gene Synonyms: Plap

Allele/Variant
Source: rs222660874
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105764619A>T
Gene Synonyms: Plap

Allele/Variant
Source: rs47263644
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105767053C>G
Gene Synonyms: Plap

Allele/Variant
Source: rs217441468
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105767164C>A
Gene Synonyms: Plap

Allele/Variant
Source: rs1131827844
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105765672G>C
Gene Synonyms: Plap

Allele/Variant
Source: rs1134049984
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105765675A>T
Gene Synonyms: Plap

Allele/Variant
Source: rs579136275
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105755045C>T
Gene Synonyms: Plap

Allele/Variant
Source: rs253714310
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105755841G>T
Gene Synonyms: Plap

Allele/Variant
Source: rs265141238
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105755907T>G
Gene Synonyms: Plap

Allele/Variant
Source: rs251504955
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105756155G>C
Gene Synonyms: Plap

Allele/Variant
Source: rs49786271
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105768951T>G
Gene Synonyms: Plap

Allele/Variant
Source: rs238682664
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105769114G>A
Gene Synonyms: Plap

Allele/Variant
Source: rs231112449
Genes: Papola (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)12:105769628G>A
Gene Synonyms: Plap