Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
(GRCh38)9:111484243C>G
(Homo sapiens)Allele/Variant
Source: rs1051139703
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484243C>G
Gene Synonyms: KIAA0368
(GRCh38)9:111484183G>A
(Homo sapiens)Allele/Variant
Source: rs781606858
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484183G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111484128C>T
(Homo sapiens)Allele/Variant
Source: rs902729815
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484128C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111372455G>T
(Homo sapiens)Allele/Variant
Source: rs779274948
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111372455G>T
Gene Synonyms: KIAA0368
(GRCh38)9:111378596G>A
(Homo sapiens)Allele/Variant
Source: rs759133299
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111378596G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111394243T>C
(Homo sapiens)Allele/Variant
Source: rs778018572
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111394243T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111437086T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111437086T>C
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111437086T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111458323C>T
(Homo sapiens)Allele/Variant
Source: rs10759497
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111458323C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111373990C>T
(Homo sapiens)Allele/Variant
Source: rs201219641
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111373990C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111383250T>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111383250T>G
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111383250T>G
Gene Synonyms: KIAA0368
(GRCh38)9:111430624T>G
(Homo sapiens)Allele/Variant
Source: rs201061247
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111430624T>G
Gene Synonyms: KIAA0368
(GRCh38)9:111369126C>G
(Homo sapiens)Allele/Variant
Source: rs1157458216
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111369126C>G
Gene Synonyms: KIAA0368
(GRCh38)9:111369155C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111369155C>T
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111369155C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111437005T>C
(Homo sapiens)Allele/Variant
Source: rs562094795
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111437005T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111437017G>A
(Homo sapiens)Allele/Variant
Source: rs377382407
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111437017G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111373316C>T
(Homo sapiens)Allele/Variant
Source: rs947043667
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111373316C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111484479G>C
(Homo sapiens)Allele/Variant
Source: rs202161291
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484479G>C
Gene Synonyms: KIAA0368
(GRCh38)9:111484036G>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111484036G>C
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484036G>C
Gene Synonyms: KIAA0368
(GRCh38)9:111484233G>A
(Homo sapiens)Allele/Variant
Source: rs930030173
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484233G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111484475G>A
(Homo sapiens)Allele/Variant
Source: rs773619592
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111484475G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111414632A>G
(Homo sapiens)Allele/Variant
Source: rs767878910
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111414632A>G
Gene Synonyms: KIAA0368
(GRCh38)9:111421988G>A
(Homo sapiens)Allele/Variant
Source: rs760760389
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111421988G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111370547T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111370547T>C
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111370547T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111440498G>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.111440498G>A
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111440498G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111442327T>C
(Homo sapiens)Allele/Variant
Source: rs201371846
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111442327T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111444463C>T
(Homo sapiens)Allele/Variant
Source: rs1460406726
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111444463C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111390001T>C
(Homo sapiens)Allele/Variant
Source: rs753213898
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111390001T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111392780A>G
(Homo sapiens)Allele/Variant
Source: rs780506510
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111392780A>G
Gene Synonyms: KIAA0368
(GRCh38)9:111408665T>C
(Homo sapiens)Allele/Variant
Source: rs765437719
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111408665T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111411099G>A
(Homo sapiens)Allele/Variant
Source: rs371781434
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111411099G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111362043T>C
(Homo sapiens)Allele/Variant
Source: rs2098113894
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111362043T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111414622C>T
(Homo sapiens)Allele/Variant
Source: rs192111516
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111414622C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111420104C>T
(Homo sapiens)Allele/Variant
Source: rs369458895
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111420104C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111366589G>A
(Homo sapiens)Allele/Variant
Source: rs745910335
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111366589G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111385383A>C
(Homo sapiens)Allele/Variant
Source: rs1470701485
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111385383A>C
Gene Synonyms: KIAA0368
(GRCh38)9:111411141C>A
(Homo sapiens)Allele/Variant
Source: rs752181912
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111411141C>A
Gene Synonyms: KIAA0368
(GRCh38)9:111416319T>C
(Homo sapiens)Allele/Variant
Source: rs373529182
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111416319T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111422136T>G
(Homo sapiens)Allele/Variant
Source: rs202113622
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111422136T>G
Gene Synonyms: KIAA0368
(GRCh38)9:111425747T>C
(Homo sapiens)Allele/Variant
Source: rs766294161
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111425747T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111433360T>C
(Homo sapiens)Allele/Variant
Source: rs375226838
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111433360T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111413929G>A
(Homo sapiens)Allele/Variant
Source: rs1235002768
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111413929G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111414602G>A
(Homo sapiens)Allele/Variant
Source: rs373640524
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111414602G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111363650G>A
(Homo sapiens)Allele/Variant
Source: rs1193814930
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111363650G>A
Gene Synonyms: KIAA0368
(GRCh38)9:111370601T>C
(Homo sapiens)Allele/Variant
Source: rs538430585
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111370601T>C
Gene Synonyms: KIAA0368
(GRCh38)9:111394228C>T
(Homo sapiens)Allele/Variant
Source: rs201479552
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111394228C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111362104T>A
(Homo sapiens)Allele/Variant
Source: rs201238185
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111362104T>A
Gene Synonyms: KIAA0368
(GRCh38)9:111422175C>T
(Homo sapiens)Allele/Variant
Source: rs1407517741
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111422175C>T
Gene Synonyms: KIAA0368
(GRCh38)9:111444440G>C
(Homo sapiens)Allele/Variant
Source: rs372260026
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111444440G>C
Gene Synonyms: KIAA0368
(GRCh38)9:111389720C>A
(Homo sapiens)Allele/Variant
Source: rs747039801
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111389720C>A
Gene Synonyms: KIAA0368
(GRCh38)9:111397057T>C
(Homo sapiens)Allele/Variant
Source: rs754808999
Genes: ECPAS (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)9:111397057T>C
Gene Synonyms: KIAA0368