Version: 8.0.0
Date: Tue Jan 28 2025
300 results for gal3st4

(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

(GRCh38)7:100166680C>T

(Homo sapiens)
Allele/Variant
Source: rs1415973188
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)7:100166680C>T

(GRCh38)7:100160676G>C

(Homo sapiens)
Allele/Variant
Source: rs149033197
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160676G>C

(GRCh38)7:100166776G>A

(Homo sapiens)
Allele/Variant
Source: rs760276260
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)7:100166776G>A

(GRCh38)7:100160331C>T

(Homo sapiens)
Allele/Variant
Source: rs3800952
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)7:100160331C>T

(GRCh38)7:100160522C>T

(Homo sapiens)
Allele/Variant
Source: rs147809354
Genes: GAL3ST4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:100160522C>T

(GRCh38)7:100160592A>G

(Homo sapiens)
Allele/Variant
Source: NC_000007.14:g.100160592A>G
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)7:100160592A>G

(mRatBN7.2)12:17272747A>G

(Rattus norvegicus)
Allele/Variant
Source: rs105161345
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272747A>G

(mRatBN7.2)12:17272360T>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.17272360T>C
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272360T>C

(mRatBN7.2)12:17272597G>T

(Rattus norvegicus)
Allele/Variant
Source: rs106827720
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272597G>T

(mRatBN7.2)12:17271631G>C

(Rattus norvegicus)
Allele/Variant
Source: NC_051347.1:g.17271631G>C
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17271631G>C

(mRatBN7.2)12:17272784C>T

(Rattus norvegicus)
Allele/Variant
Source: rs63873103
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272784C>T

(mRatBN7.2)12:17276917T>C

(Rattus norvegicus)
Allele/Variant
Source: rs106541711
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17276917T>C

(mRatBN7.2)12:17272555A>G

(Rattus norvegicus)
Allele/Variant
Source: rs107487584
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272555A>G

(mRatBN7.2)12:17272586A>G

(Rattus norvegicus)
Allele/Variant
Source: rs104974986
Genes: Gal3st4 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)12:17272586A>G