283 results
Allele/Variant Genes: inha (Dre)

umo19

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-200630-3
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5200840913
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21086594T>C

Allele/Variant
Source: ss5200840624
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21072703T>C

Allele/Variant
Source: ss5200840647
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21075100T>G

Allele/Variant
Source: ss5200840632
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21077499A>C

Allele/Variant
Source: ss5200840691
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21077647G>C

Allele/Variant
Source: ss5200840896
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21088089G>A

Allele/Variant
Source: ss5200840870
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21089467T>G

Allele/Variant
Source: ss5200840833
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21090807A>G

Allele/Variant
Source: ss5200840775
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083925A>G

Allele/Variant
Source: ss5200840855
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21085052T>C

Allele/Variant
Source: ss5200840565
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070218C>A

Allele/Variant
Source: ss5200840544
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070327A>C

Allele/Variant
Source: ss5200840564
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070648T>A

Allele/Variant
Source: ss5200840550
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071059C>T

Allele/Variant
Source: ss5200840540
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071081C>T

Allele/Variant
Source: ss5200840707
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071338G>A

Allele/Variant
Source: ss5200840676
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071460C>T

Allele/Variant
Source: ss5200840795
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083427C>T

Allele/Variant
Source: ss5200840763
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083543C>G

Allele/Variant
Source: ss5200840755
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083651T>C

Allele/Variant
Source: ss5200840668
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071515A>C

Allele/Variant
Source: ss5200840635
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071716A>C

Allele/Variant
Source: ss5200840806
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083913T>C

Allele/Variant
Source: ss5200840825
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21084926G>T

Allele/Variant
Source: ss5200840792
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21079486C>T

Allele/Variant
Source: ss5200840866
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21086610T>A

Allele/Variant
Source: ss5200840848
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21089048A>C

Allele/Variant
Source: ss5200840903
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21089079A>T

Allele/Variant
Source: ss5200840578
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070215A>T

Allele/Variant
Source: ss5200840622
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071096G>T

Allele/Variant
Source: ss5200840779
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083718C>T

Allele/Variant
Source: ss5200840807
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21083766G>A

Allele/Variant
Source: ss5200840774
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21084178G>A

Allele/Variant
Source: ss5200840844
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21084777C>T

Allele/Variant
Source: ss5200840869
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21084904G>A

Allele/Variant
Source: ss5200840890
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21084973T>C

Allele/Variant
Source: ss5200840701
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21072829C>T

Allele/Variant
Source: ss5200840703
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21073772A>G

Allele/Variant
Source: ss5200840709
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21073786A>C

Allele/Variant
Source: ss5200840729
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21078499C>G

Allele/Variant
Source: ss5200840523
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21069765T>C

Allele/Variant
Source: ss5200840615
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070252T>A

Allele/Variant
Source: ss5200840568
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070260A>G

Allele/Variant
Source: ss5200840577
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070588G>T

Allele/Variant
Source: ss5200840572
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070672T>G

Allele/Variant
Source: ss5200840527
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21070830G>T

Allele/Variant
Source: ss5200840596
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071125T>G

Allele/Variant
Source: ss5200840529
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071148T>A

Allele/Variant
Source: ss5200840699
Genes: inha (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)6:21071320A>T