201 results
Allele/Variant Genes: bcl9 (Dre)
Allele/Variant
Source: ss5199597792
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47334200A>G

Allele/Variant
Source: ss5199597848
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47336533T>C

Allele/Variant
Source: ss5199597891
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47337200A>G

Allele/Variant
Source: ss5199597865
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47340825C>T

Allele/Variant
Source: ss5199597736
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333454A>T

Allele/Variant
Source: ss5199597735
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333476A>C

Allele/Variant
Source: ss5199597778
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333511C>T

Allele/Variant
Source: ss5199597708
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333781C>T

Allele/Variant
Source: ss5199597858
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47336977T>C

Allele/Variant
Source: ss5199597897
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341496A>T

zh714

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171220-1
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: deletion
Molecular Consequence: frameshift_variant
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199597846
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47338818T>C

Allele/Variant
Source: ss5199597791
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47331790A>G

Allele/Variant
Source: ss5199597773
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333364G>A

Allele/Variant
Source: ss5199597742
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333450C>T

Allele/Variant
Source: ss5199597757
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333693T>C

Allele/Variant
Source: ss5199597716
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333910C>G

Allele/Variant
Source: ss5199597771
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333966T>C

Allele/Variant
Source: ss5199597881
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47336055A>G

Allele/Variant
Source: ss5199597854
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47336233G>T

Allele/Variant
Source: ss5199597812
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47340532A>G

sa13893

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-12307
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199597997
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341931A>G

Allele/Variant
Source: ss5199597976
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47342642G>T

Allele/Variant
Source: ss5199597991
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47344328C>T

Allele/Variant
Source: ss5199597709
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333526A>C

Allele/Variant
Source: ss5199597775
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333623T>A

Allele/Variant
Source: ss5199597776
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47334642A>T

Allele/Variant
Source: ss5199597935
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341799T>C

Allele/Variant
Source: ss5199597961
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47342351C>A

Allele/Variant
Source: ss5199597828
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47338056C>T

Allele/Variant
Source: ss5199597835
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47338141A>G

Allele/Variant
Source: ss5199597743
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333232A>G

Allele/Variant
Source: ss5199597729
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333497C>T

Allele/Variant
Source: ss5199597753
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333563A>T

Allele/Variant
Source: ss5199597764
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333565A>C

Allele/Variant
Source: ss5199597797
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47333740A>T

Allele/Variant
Source: ss5199597861
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47336178G>T

Allele/Variant
Source: ss5199597862
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47340921C>T

Allele/Variant
Source: ss5199597807
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341021C>T

Allele/Variant
Source: ss5199597851
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341520T>C

Allele/Variant
Source: ss5199597934
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47342273C>A

Allele/Variant
Source: ss5199597920
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47342631A>T

Allele/Variant
Source: ss5199597850
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47337750A>T

Allele/Variant
Source: ss5199597824
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47337940A>C

Allele/Variant
Source: ss5199597829
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47340550T>A

Allele/Variant
Source: ss5199597825
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47340830G>A

Allele/Variant
Source: ss5199597836
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341190A>G

Allele/Variant
Source: ss5199597817
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341515T>C

Allele/Variant
Source: ss5199597984
Genes: bcl9 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:47341672C>T