Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Allele/Variant
la011695Tg
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-130129-2091
Genes: gpc2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: gal3st4
sa20945
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131220-318
Genes: gal3st4 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: gal3st4 (Dre)
sa22397
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131217-16504
Genes: gpc2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: gal3st4
(GRCh38)7:100160116G>T
(Homo sapiens)Allele/Variant
Source: rs200159207
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160116G>T
(GRCh38)7:100166569G>A
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.100166569G>A
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166569G>A
(GRCh38)7:100166707T>G
(Homo sapiens)Allele/Variant
Source: rs777963100
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166707T>G
(GRCh38)7:100160773C>T
(Homo sapiens)Allele/Variant
Source: rs200053288
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160773C>T
(GRCh38)7:100160782C>T
(Homo sapiens)Allele/Variant
Source: rs768637210
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160782C>T
(GRCh38)7:100160811C>T
(Homo sapiens)Allele/Variant
Source: rs774937557
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160811C>T
(GRCh38)7:100160226C>T
(Homo sapiens)Allele/Variant
Source: rs762070602
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160226C>T
(GRCh38)7:100160508A>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.100160508A>G
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160508A>G
(GRCh38)7:100160031C>T
(Homo sapiens)Allele/Variant
Source: rs144461733
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160031C>T
(GRCh38)7:100160206C>T
(Homo sapiens)Allele/Variant
Source: rs1456158446
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160206C>T
(GRCh38)7:100160681G>T
(Homo sapiens)Allele/Variant
Source: rs748647653
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160681G>T
(GRCh38)7:100166658G>T
(Homo sapiens)Allele/Variant
Source: rs760360297
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166658G>T
(GRCh38)7:100167064C>T
(Homo sapiens)Allele/Variant
Source: rs752372982
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100167064C>T
(GRCh38)7:100160307G>C
(Homo sapiens)Allele/Variant
Source: rs1364763696
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160307G>C
(GRCh38)7:100160417G>A
(Homo sapiens)Allele/Variant
Source: rs140652132
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160417G>A
(GRCh38)7:100160484A>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.100160484A>G
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160484A>G
(GRCh38)7:100160653C>G
(Homo sapiens)Allele/Variant
Source: rs775899842
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160653C>G
(GRCh38)7:100160946A>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.100160946A>G
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160946A>G
(GRCh38)7:100160257A>G
(Homo sapiens)Allele/Variant
Source: rs755375291
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160257A>G
(GRCh38)7:100166510G>T
(Homo sapiens)Allele/Variant
Source: rs777894947
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166510G>T
(GRCh38)7:100166493A>T
(Homo sapiens)Allele/Variant
Source: rs149092760
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166493A>T
(GRCh38)7:100160700T>A
(Homo sapiens)Allele/Variant
Source: rs770433938
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160700T>A
(GRCh38)7:100160851G>A
(Homo sapiens)Allele/Variant
Source: rs374392589
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160851G>A
(GRCh38)7:100159975G>C
(Homo sapiens)Allele/Variant
Source: rs149961692
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100159975G>C
(GRCh38)7:100160236C>T
(Homo sapiens)Allele/Variant
Source: rs766932470
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160236C>T
(GRCh38)7:100160535G>T
(Homo sapiens)Allele/Variant
Source: rs149908309
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160535G>T
(GRCh38)7:100166761C>T
(Homo sapiens)Allele/Variant
Source: rs779838710
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166761C>T
(GRCh38)7:100166669G>A
(Homo sapiens)Allele/Variant
Source: rs376538136
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166669G>A
(GRCh38)7:100160551C>T
(Homo sapiens)Allele/Variant
Source: rs144870417
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160551C>T
(GRCh38)7:100160217G>A
(Homo sapiens)Allele/Variant
Source: rs776755474
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160217G>A
(GRCh38)7:100159985C>A
(Homo sapiens)Allele/Variant
Source: rs765114251
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100159985C>A
(GRCh38)7:100160116G>A
(Homo sapiens)Allele/Variant
Source: rs200159207
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160116G>A
(GRCh38)7:100166572C>T
(Homo sapiens)Allele/Variant
Source: rs763411487
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166572C>T
(GRCh38)7:100166626C>T
(Homo sapiens)Allele/Variant
Source: rs200571320
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166626C>T
(GRCh38)7:100166668C>T
(Homo sapiens)Allele/Variant
Source: rs373254633
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166668C>T
(GRCh38)7:100166999G>A
(Homo sapiens)Allele/Variant
Source: rs1799085397
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166999G>A
(GRCh38)7:100160316C>T
(Homo sapiens)Allele/Variant
Source: rs138298556
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160316C>T
(GRCh38)7:100160332G>A
(Homo sapiens)Allele/Variant
Source: rs112880621
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160332G>A
(GRCh38)7:100160777G>C
(Homo sapiens)Allele/Variant
Source: rs368643591
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160777G>C
(GRCh38)7:100166749G>T
(Homo sapiens)Allele/Variant
Source: rs368429546
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166749G>T
(GRCh38)7:100160506C>G
(Homo sapiens)Allele/Variant
Source: rs750043430
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160506C>G
(GRCh38)7:100166617A>G
(Homo sapiens)Allele/Variant
Source: rs142988850
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166617A>G
(GRCh38)7:100160904G>A
(Homo sapiens)Allele/Variant
Source: rs550951408
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160904G>A
(GRCh38)7:100160410C>T
(Homo sapiens)Allele/Variant
Source: rs757897746
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160410C>T
(GRCh38)7:100160158C>T
(Homo sapiens)Allele/Variant
Source: rs754074041
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160158C>T
(GRCh38)7:100166614C>T
(Homo sapiens)Allele/Variant
Source: rs201437336
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166614C>T
(GRCh38)7:100166651C>T
(Homo sapiens)Allele/Variant
Source: rs115841575
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100166651C>T