Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Construct Expressed Component
Construct Regulatory Region
Allele/Variant
(GRCh38)19:46845980G>A
(Homo sapiens)Allele/Variant
Source: rs1482361949
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845980G>A
(GRCh38)19:46838512C>T
(Homo sapiens)Allele/Variant
Source: rs1266748065
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838512C>T
(GRCh38)19:46839523C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839523C>T
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839523C>T
(GRCh38)19:46846080C>G
(Homo sapiens)Allele/Variant
Source: rs1001192722
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846080C>G
(GRCh38)19:46838532T>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46838532T>C
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838532T>C
(GRCh38)19:46838764C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46838764C>T
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838764C>T
(GRCh38)19:46839496G>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839496G>A
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839496G>A
(GRCh38)19:46839610A>G
(Homo sapiens)Allele/Variant
Source: rs312185
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839610A>G
(GRCh38)19:46846116C>T
(Homo sapiens)Allele/Variant
Source: rs374421844
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846116C>T
(GRCh38)19:46839543A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839543A>G
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839543A>G
(GRCh38)19:46846102C>T
(Homo sapiens)Allele/Variant
Source: rs397514499
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846102C>T
(GRCh38)19:46838570G>A
(Homo sapiens)Allele/Variant
Source: rs45527038
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838570G>A
(GRCh38)19:46839460C>T
(Homo sapiens)Allele/Variant
Source: rs312186
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839460C>T
(GRCh38)19:46839063G>C
(Homo sapiens)Allele/Variant
Source: rs117536527
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839063G>C
(GRCh38)19:46839482T>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839482T>C
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839482T>C
(GRCh38)19:46839553C>T
(Homo sapiens)Allele/Variant
Source: rs1057522809
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839553C>T
(GRCh38)19:46839607G>A
(Homo sapiens)Allele/Variant
Source: rs534575535
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839607G>A
(GRCh38)19:46839457C>T
(Homo sapiens)Allele/Variant
Source: rs185343764
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839457C>T
(GRCh38)19:46839458G>A
(Homo sapiens)Allele/Variant
Source: rs1172216017
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839458G>A
(GRCh38)19:46839567A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839567A>G
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839567A>G
(GRCh38)19:46846016C>T
(Homo sapiens)Allele/Variant
Source: rs539480372
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846016C>T
(GRCh38)19:46846050G>A
(Homo sapiens)Allele/Variant
Source: rs376074817
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846050G>A
(GRCh38)19:46838516A>C
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46838516A>C
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838516A>C
(GRCh38)19:46839434C>T
(Homo sapiens)Allele/Variant
Source: rs181763835
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839434C>T
(GRCh38)19:46838578G>A
(Homo sapiens)Allele/Variant
Source: rs541382293
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838578G>A
(GRCh38)19:46846149G>A
(Homo sapiens)Allele/Variant
Source: rs368803584
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846149G>A
(GRCh38)19:46846102C>A
(Homo sapiens)Allele/Variant
Source: rs397514499
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846102C>A
(GRCh38)19:46846137G>C
(Homo sapiens)Allele/Variant
Source: rs1281403558
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846137G>C
(GRCh38)19:46846150C>A
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46846150C>A
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846150C>A
(GRCh38)19:46846191G>A
(Homo sapiens)Allele/Variant
Source: rs370660532
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846191G>A
(GRCh38)19:46845984G>A
(Homo sapiens)Allele/Variant
Source: rs1244143500
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845984G>A
(GRCh38)19:46846071A>G
(Homo sapiens)Allele/Variant
Source: rs150080027
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846071A>G
(GRCh38)19:46838627C>A
(Homo sapiens)Allele/Variant
Source: rs147698652
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838627C>A
(GRCh38)19:46846147G>A
(Homo sapiens)Allele/Variant
Source: rs555604346
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846147G>A
(GRCh38)19:46846098C>T
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46846098C>T
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846098C>T
(GRCh38)19:46838513G>A
(Homo sapiens)Allele/Variant
Source: rs762532614
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838513G>A
(GRCh38)19:46838519C>T
(Homo sapiens)Allele/Variant
Source: rs751283401
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838519C>T
(GRCh38)19:46838541G>A
(Homo sapiens)Allele/Variant
Source: rs756038304
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838541G>A
(GRCh38)19:46838782G>A
(Homo sapiens)Allele/Variant
Source: rs773768685
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838782G>A
(GRCh38)19:46846131G>A
(Homo sapiens)Allele/Variant
Source: rs201984742
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846131G>A
(GRCh38)19:46846041C>T
(Homo sapiens)Allele/Variant
Source: rs943777438
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846041C>T
(GRCh38)19:46846118G>A
(Homo sapiens)Allele/Variant
Source: rs1064795235
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846118G>A
(GRCh38)19:46838773G>A
(Homo sapiens)Allele/Variant
Source: rs770400521
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838773G>A
(GRCh38)19:46839491G>A
(Homo sapiens)Allele/Variant
Source: rs377069919
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839491G>A
(GRCh38)19:46850744G>T
(Homo sapiens)Allele/Variant
Source: rs1396339539
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46850744G>T
(GRCh38)19:46846017G>A
(Homo sapiens)Allele/Variant
Source: rs374514769
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846017G>A
(GRCh38)19:46846074A>G
(Homo sapiens)Allele/Variant
Source: rs2122792537
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846074A>G
(GRCh38)19:46838237G>A
(Homo sapiens)Allele/Variant
Source: rs17653
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838237G>A
(GRCh38)19:46838377C>T
(Homo sapiens)Allele/Variant
Source: rs76955283
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838377C>T
(GRCh38)19:46838490G>A
(Homo sapiens)Allele/Variant
Source: rs2055451979
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838490G>A