Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant
Species
Category
Variant Type
Molecular Consequence
Genes
Construct Expressed Component
Construct Knockdown Component
Construct Regulatory Region
Allele/Variant
(R6)2L:22584762C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22584762C>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22584762C>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22585155C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22585155C>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22585155C>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22579538G>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22579538G>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22579538G>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22581867A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22581867A>G
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22581867A>G
Gene Synonyms: slmap...SLMAP
(R6)2L:22580121T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580121T>C
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:22580121T>C
Gene Synonyms: slmap...SLMAP
(R6)2L:22580640A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580640A>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:22580640A>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22580734A>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580734A>G
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22580734A>G
Gene Synonyms: slmap...SLMAP
(R6)2L:22580876T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580876T>C
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22580876T>C
Gene Synonyms: slmap...SLMAP
(R6)2L:22580959T>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580959T>G
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22580959T>G
Gene Synonyms: slmap...SLMAP
(R6)2L:22581611C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22581611C>A
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22581611C>A
Gene Synonyms: slmap...SLMAP
(R6)2L:22581708C>G
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22581708C>G
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22581708C>G
Gene Synonyms: slmap...SLMAP
(R6)2L:22584096A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22584096A>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22584096A>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22584966C>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22584966C>A
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22584966C>A
Gene Synonyms: slmap...SLMAP
(R6)2L:22585684G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22585684G>C
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:22585684G>C
Gene Synonyms: slmap...SLMAP
(R6)2L:22580141G>A
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580141G>A
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:22580141G>A
Gene Synonyms: slmap...SLMAP
(R6)2L:22580085A>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580085A>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:22580085A>T
Gene Synonyms: slmap...SLMAP
(R6)2L:22580330G>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22580330G>C
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:22580330G>C
Gene Synonyms: slmap...SLMAP
(R6)2L:22581859T>C
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22581859T>C
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:22581859T>C
Gene Synonyms: slmap...SLMAP
(R6)2L:22585368C>T
(Drosophila melanogaster)Allele/Variant
Source: NT_033779.5:g.22585368C>T
Genes: Slmap (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:22585368C>T
Gene Synonyms: slmap...SLMAP
sa41914
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-7796
Genes: slmapa (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: slmapa (Dre)
sa30953
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-735
Genes: slmapa (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available
Genes: slmapa (Dre)
sa21976
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-131217-16250
Genes: slmapa (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: slmapa (Dre)
sa43948
(Danio rerio)Allele/Variant
Source: ZFIN:ZDB-ALT-160601-9390
Genes: slmapb (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available
Gene Synonyms: slmap
Genes: slmapb (Dre)
(GRCh38)3:57757801G>A
(Homo sapiens)Allele/Variant
Source: rs781119976
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57757801G>A
(GRCh38)3:57831464C>G
(Homo sapiens)Allele/Variant
Source: rs1295613390
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57831464C>G
(GRCh38)3:57757693G>T
(Homo sapiens)Allele/Variant
Source: rs760264345
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57757693G>T
(GRCh38)3:57841360G>T
(Homo sapiens)Allele/Variant
Source: rs145924069
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841360G>T
(GRCh38)3:57841364C>T
(Homo sapiens)Allele/Variant
Source: rs748820617
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841364C>T
(GRCh38)3:57841538A>G
(Homo sapiens)Allele/Variant
Source: rs116002844
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841538A>G
(GRCh38)3:57847180T>A
(Homo sapiens)Allele/Variant
Source: rs536292946
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847180T>A
(GRCh38)3:57847181A>T
(Homo sapiens)Allele/Variant
Source: rs2153574252
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847181A>T
(GRCh38)3:57847211C>A
(Homo sapiens)Allele/Variant
Source: rs1159969169
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847211C>A
(GRCh38)3:57909163C>T
(Homo sapiens)Allele/Variant
Source: rs1009843149
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57909163C>T
(GRCh38)3:57860820G>C
(Homo sapiens)Allele/Variant
Source: rs1211281068
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57860820G>C
(GRCh38)3:57860837G>A
(Homo sapiens)Allele/Variant
Source: rs146606397
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57860837G>A
(GRCh38)3:57862048G>A
(Homo sapiens)Allele/Variant
Source: rs754387957
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862048G>A
(GRCh38)3:57862057G>A
(Homo sapiens)Allele/Variant
Source: rs1424987573
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862057G>A
(GRCh38)3:57864644G>A
(Homo sapiens)Allele/Variant
Source: rs149548827
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57864644G>A
(GRCh38)3:57871616G>A
(Homo sapiens)Allele/Variant
Source: rs775405372
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57871616G>A
(GRCh38)3:57890077T>C
(Homo sapiens)Allele/Variant
Source: rs547267872
Genes: SLMAP (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)3:57890077T>C
(GRCh38)3:57896893G>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57896893G>T
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896893G>T
(GRCh38)3:57907933G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57907933G>A
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57907933G>A
(GRCh38)3:57907954C>G
(Homo sapiens)Allele/Variant
Source: rs775234969
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57907954C>G
(GRCh38)3:57871687T>C
(Homo sapiens)Allele/Variant
Source: rs375841302
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57871687T>C
(GRCh38)3:57896936C>T
(Homo sapiens)Allele/Variant
Source: rs539985706
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896936C>T
(GRCh38)3:57907962A>C
(Homo sapiens)Allele/Variant
Source: rs2096607956
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57907962A>C
(GRCh38)3:57912479G>A
(Homo sapiens)Allele/Variant
Source: rs753780730
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912479G>A
(GRCh38)3:57912524C>T
(Homo sapiens)Allele/Variant
Source: rs1379169914
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912524C>T
(GRCh38)3:57927370G>A
(Homo sapiens)Allele/Variant
Source: rs557921655
Genes: SLMAP (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)3:57927370G>A
(GRCh38)3:57927406G>A
(Homo sapiens)Allele/Variant
Source: rs149054976
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57927406G>A