Version: 8.0.0
Date: Tue Jan 28 2025
556 results for AP2S1
Allele/Variant Construct Regulatory Region: hsp70l (Dre)

Ap2s1em1Rvt

(Mus musculus)
Allele/Variant
Source: MGI:7408432
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1em1Rvt

Ap2s1em1(IMPC)Tcp

(Mus musculus)
Allele/Variant
Source: MGI:5754583
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1em1(IMPC)Tcp

Ap2s1em5H

(Mus musculus)
Allele/Variant
Source: MGI:7430828
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1em5H

Ap2s1em5Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7309904
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1em5Gpt

Ap2s1em2(IMPC)Tcp

(Mus musculus)
Allele/Variant
Source: MGI:6316162
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1em2(IMPC)Tcp

Ap2s1m3Rvt

(Mus musculus)
Allele/Variant
Source: MGI:6401510
Genes: Ap2s1 (Mmu)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Symbol: Ap2s1 (Mmu)
Genes: Ap2s1 (Mmu)
Symbol: Ap2s1m3Rvt

hv1

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-240305-1
Genes: ap2s1 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: ap2s1 (Dre)

hv2Tg

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-240305-2
Genes: Not Available
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Construct Expressed Component: ap2s1 (Dre)

p172

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-150701-2
Genes: ap2s1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: ap2s1 (Dre)

p199

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-180129-11
Genes: ap2s1 (Dre)
Synonyms: Not Available
Variant Type: delins
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available
Genes: ap2s1 (Dre)

(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)19:46838825A>C

(Homo sapiens)
Allele/Variant
Source: rs2122754014
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838825A>C

(GRCh38)19:46839156G>A

(Homo sapiens)
Allele/Variant
Source: rs111997019
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839156G>A

(GRCh38)19:46839461G>A

(Homo sapiens)
Allele/Variant
Source: rs776590608
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)19:46839461G>A

(GRCh38)19:46839527T>C

(Homo sapiens)
Allele/Variant
Source: rs2055478520
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)19:46839527T>C

(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)19:46838765A>G

(Homo sapiens)
Allele/Variant
Source: rs1555748483
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838765A>G

(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)19:46845979G>A

(Homo sapiens)
Allele/Variant
Source: rs746517943
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845979G>A

(GRCh38)19:46845988G>A

(Homo sapiens)
Allele/Variant
Source: rs747850028
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845988G>A

(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)19:46839446C>T

(Homo sapiens)
Allele/Variant
Source: rs199770574
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839446C>T

(GRCh38)19:46846022G>C

(Homo sapiens)
Allele/Variant
Source: NC_000019.10:g.46846022G>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)19:46846022G>C

(GRCh38)19:46850744G>A

(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>A

(GRCh38)19:46850750C>A

(Homo sapiens)
Allele/Variant
Source: rs1568451783
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)19:46850750C>A

(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)19:46850753T>C

(Homo sapiens)
Allele/Variant
Source: rs772626569
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)19:46850753T>C

(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)19:46850126C>T

(Homo sapiens)
Allele/Variant
Source: rs557497251
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)19:46850126C>T

(GRCh38)19:46839551G>A

(Homo sapiens)
Allele/Variant
Source: rs2122759002
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)19:46839551G>A

(GRCh38)19:46838160C>T

(Homo sapiens)
Allele/Variant
Source: rs142218524
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838160C>T

(GRCh38)19:46850751G>C

(Homo sapiens)
Allele/Variant
Source: rs759974290
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)19:46850751G>C

(GRCh38)19:46838558G>A

(Homo sapiens)
Allele/Variant
Source: rs1463007928
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838558G>A

(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)19:46845976C>T

(Homo sapiens)
Allele/Variant
Source: rs1407800358
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845976C>T

(GRCh38)19:46845987C>T

(Homo sapiens)
Allele/Variant
Source: rs201686470
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46845987C>T

(GRCh38)19:46846021C>T

(Homo sapiens)
Allele/Variant
Source: rs2122792210
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)19:46846021C>T

(GRCh38)19:46846103G>A

(Homo sapiens)
Allele/Variant
Source: rs397514498
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)19:46846103G>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)19:46838559G>A

(Homo sapiens)
Allele/Variant
Source: rs1363807535
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838559G>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)19:46839550C>T

(Homo sapiens)
Allele/Variant
Source: rs754997253
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)19:46839550C>T

(GRCh38)19:46839822C>A

(Homo sapiens)
Allele/Variant
Source: rs116743544
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46839822C>A

(GRCh38)19:46838542T>A

(Homo sapiens)
Allele/Variant
Source: rs779087525
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46838542T>A

(GRCh38)19:46838805A>G

(Homo sapiens)
Allele/Variant
Source: rs1248312229
Genes: AP2S1 (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)19:46838805A>G

(GRCh38)19:46838807A>C

(Homo sapiens)
Allele/Variant
Source: rs2055458627
Genes: AP2S1 (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)19:46838807A>C

(GRCh38)19:46846162A>T

(Homo sapiens)
Allele/Variant
Source: rs749113308
Genes: AP2S1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)19:46846162A>T

(GRCh38)19:46846117C>T

(Homo sapiens)
Allele/Variant
Source: rs1297109231
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)19:46846117C>T

(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)19:46845980G>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