Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Molecular Consequence: synonymous variant
(GRCh38)19:46838489C>T
(Homo sapiens)Allele/Variant
Source: rs762267195
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838489C>T
(GRCh38)19:46839597G>A
(Homo sapiens)Allele/Variant
Source: rs778066242
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)19:46839597G>A
(GRCh38)19:46838791G>A
(Homo sapiens)Allele/Variant
Source: rs143384246
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838791G>A
(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)19:46846116C>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)19:46838540C>T
(Homo sapiens)Allele/Variant
Source: rs752653383
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838540C>T
(GRCh38)19:46846035G>A
(Homo sapiens)Allele/Variant
Source: rs368988346
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)19:46846035G>A
(GRCh38)19:46838770A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46838770A>G
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838770A>G
(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)19:46839471G>A
(Homo sapiens)Allele/Variant
Source: rs151335841
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)19:46839471G>A
(GRCh38)19:46846104C>T
(Homo sapiens)Allele/Variant
Source: rs754039002
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)19:46846104C>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)19:46846137G>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)19:46846071A>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)19:46846098C>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)19:46838782G>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)19:46839546A>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839546A>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)19:46839546A>G
(GRCh38)19:46839573C>G
(Homo sapiens)Allele/Variant
Source: NC_000019.10:g.46839573C>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)19:46839573C>G
(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)19:46838773G>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)19:46846017G>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)19:46846026G>A
(Homo sapiens)Allele/Variant
Source: rs890897569
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)19:46846026G>A
(GRCh38)19:46846128G>A
(Homo sapiens)Allele/Variant
Source: rs376700130
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)19:46846128G>A
(GRCh38)19:46846104C>A
(Homo sapiens)Allele/Variant
Source: rs754039002
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)19:46846104C>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
(GRCm39)7:16477158T>C
(Mus musculus)Allele/Variant
Source: rs234687854
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)7:16477158T>C
(GRCm39)7:16482908G>A
(Mus musculus)Allele/Variant
Source: rs248402552
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)7:16482908G>A
(GRCm39)7:16481275C>T
(Mus musculus)Allele/Variant
Source: rs13468345
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)7:16481275C>T
(GRCm39)7:16477188G>A
(Mus musculus)Allele/Variant
Source: rs50042076
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)7:16477188G>A
(GRCm39)7:16481221T>C
(Mus musculus)Allele/Variant
Source: rs50982202
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)7:16481221T>C
(mRatBN7.2)1:77427386C>T
(Rattus norvegicus)Allele/Variant
Source: rs3318940096
Genes: Ap2s1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)1:77427386C>T