Version: 8.0.0
Date: Tue Jan 28 2025
150 results
Allele/Variant Genes: CG13795 (Dme)

CG13795NP1245

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0222190
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

CG13795CR60297-TG4.1

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0404622
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

CG13795CR01393-TG4.1

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0356597
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(R6)2L:7723284T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723284T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723284T>C

(R6)2L:7725062A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725062A>G
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725062A>G

(R6)2L:7725081C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725081C>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725081C>T

(R6)2L:7724565G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724565G>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7724565G>T

(R6)2L:7724593G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724593G>A
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:7724593G>A

(R6)2L:7724606C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724606C>T
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724606C>T

(R6)2L:7724729T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724729T>C
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724729T>C

(R6)2L:7723085A>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723085A>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723085A>C

(R6)2L:7723106T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723106T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723106T>A

(R6)2L:7723364C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723364C>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723364C>T

(R6)2L:7723050A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723050A>G
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723050A>G

(R6)2L:7723124T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723124T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723124T>A

(R6)2L:7723940A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723940A>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7723940A>T

(R6)2L:7724236T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724236T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7724236T>C

(R6)2L:7724242C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724242C>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7724242C>T

(R6)2L:7723502G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723502G>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723502G>A

(R6)2L:7723733T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723733T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7723733T>C

(R6)2L:7723230T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723230T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723230T>A

(R6)2L:7723408G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723408G>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723408G>T

(R6)2L:7725076T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725076T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725076T>A

(R6)2L:7726156G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7726156G>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7726156G>A

(R6)2L:7725069A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725069A>G
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725069A>G

(R6)2L:7725504A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725504A>G
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725504A>G

(R6)2L:7723496A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723496A>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723496A>T

(R6)2L:7723643C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723643C>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7723643C>T

(R6)2L:7726289G>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7726289G>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7726289G>C

(R6)2L:7724319T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724319T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7724319T>C

(R6)2L:7724667A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724667A>G
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724667A>G

(R6)2L:7723497A>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723497A>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723497A>C

(R6)2L:7723819A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723819A>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)2L:7723819A>T

CG13795MI12420

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0298142
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: splice_region_variant, coding_sequence_variant
Diseases: Not Available
Variant Name: Not Available

(R6)2L:7723444T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723444T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723444T>C

(R6)2L:7726224T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7726224T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7726224T>A

(R6)2L:7724906G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724906G>T
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724906G>T

(R6)2L:7723688T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723688T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7723688T>C

(R6)2L:7726147G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7726147G>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7726147G>A

(R6)2L:7723407T>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723407T>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7723407T>A

(R6)2L:7725181T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725181T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7725181T>C

(R6)2L:7725267T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725267T>C
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725267T>C

(R6)2L:7724675C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724675C>T
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724675C>T

(R6)2L:7723930G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7723930G>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7723930G>A

(R6)2L:7725029G>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725029G>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)2L:7725029G>T

(R6)2L:7725063A>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7725063A>T
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)2L:7725063A>T

(R6)2L:7726293G>A

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7726293G>A
Genes: CG13795 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)2L:7726293G>A

(R6)2L:7724621A>G

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724621A>G
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724621A>G

(R6)2L:7724756C>T

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724756C>T
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724756C>T

(R6)2L:7724936T>C

(Drosophila melanogaster)
Allele/Variant
Source: NT_033779.5:g.7724936T>C
Genes: CG13795 (Dme), asRNA:CR46074 (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (R6)2L:7724936T>C