Version: 8.0.0
Date: Tue Jan 28 2025
104 results
Allele/Variant Genes: X11L (Dme)

X11L80

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0304609
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(R6)X:17604872C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17604872C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17604872C>T

(R6)X:17600006G>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17600006G>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17600006G>C

(R6)X:17600068T>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17600068T>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17600068T>A

(R6)X:17606369T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606369T>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606369T>G

(R6)X:17606529T>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606529T>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606529T>A

(R6)X:17606560A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606560A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606560A>G

(R6)X:17603115A>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603115A>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603115A>C

(R6)X:17604319G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17604319G>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17604319G>A

(R6)X:17604521G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17604521G>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17604521G>A

(R6)X:17605092A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17605092A>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17605092A>T

(R6)X:17599868C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17599868C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17599868C>T

(R6)X:17600917C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17600917C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17600917C>T

(R6)X:17602973A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17602973A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17602973A>G

(R6)X:17603045T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603045T>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17603045T>C

(R6)X:17603690T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603690T>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603690T>C

(R6)X:17603870A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603870A>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603870A>T

(R6)X:17599634C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17599634C>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17599634C>G

(R6)X:17606383G>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606383G>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606383G>C

(R6)X:17600226C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17600226C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17600226C>T

(R6)X:17602074C>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17602074C>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17602074C>G

X11Le03317

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0159534
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

(R6)X:17604067C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17604067C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (R6)X:17604067C>T

(R6)X:17605772C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17605772C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17605772C>T

(R6)X:17606035C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606035C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606035C>T

(R6)X:17599923T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17599923T>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17599923T>C

(R6)X:17601145T>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601145T>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17601145T>A

(R6)X:17601251C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601251C>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17601251C>A

(R6)X:17602457C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17602457C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17602457C>T

(R6)X:17602826G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17602826G>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17602826G>A

(R6)X:17603416A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603416A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17603416A>G

(R6)X:17603563A>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603563A>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603563A>T

X11LG538

(Drosophila melanogaster)
Allele/Variant
Source: FB:FBal0372643
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: insertion
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available

(R6)X:17600928A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17600928A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17600928A>G

(R6)X:17601503C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601503C>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17601503C>A

(R6)X:17601666G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601666G>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17601666G>T

(R6)X:17601792C>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601792C>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17601792C>A

(R6)X:17602689A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17602689A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (R6)X:17602689A>G

(R6)X:17605852T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17605852T>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17605852T>C

(R6)X:17606340C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17606340C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17606340C>T

(R6)X:17599880T>C

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17599880T>C
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17599880T>C

(R6)X:17599970G>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17599970G>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17599970G>T

(R6)X:17601349T>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601349T>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17601349T>G

(R6)X:17603525C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603525C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603525C>T

(R6)X:17601346C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601346C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17601346C>T

(R6)X:17601700A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17601700A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17601700A>G

(R6)X:17603893C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17603893C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (R6)X:17603893C>T

(R6)X:17604337G>A

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17604337G>A
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (R6)X:17604337G>A

(R6)X:17605410A>G

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17605410A>G
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17605410A>G

(R6)X:17605868C>T

(Drosophila melanogaster)
Allele/Variant
Source: NC_004354.4:g.17605868C>T
Genes: X11L (Dme)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (R6)X:17605868C>T