51 results
Allele/Variant Genes: hspa1b (Dre)
Allele/Variant
Source: ss5201250953
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968899C>T

Allele/Variant
Source: ss5201251064
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970040C>T

Allele/Variant
Source: ss5201251076
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970559A>G

Allele/Variant
Source: ss5201251034
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970581A>T

Allele/Variant
Source: ss5201251049
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970582A>T

Allele/Variant
Source: ss5201251071
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970549T>A

Allele/Variant
Source: ss5201251107
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970323A>G

Allele/Variant
Source: ss5201251085
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970471G>A

Allele/Variant
Source: ss5201250957
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968863C>T

Allele/Variant
Source: ss5201250941
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968953A>G

Allele/Variant
Source: ss5201250970
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968980T>G

Allele/Variant
Source: ss5201251035
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970470T>A

Allele/Variant
Source: ss5201251105
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970474T>A

Allele/Variant
Source: ss5201251098
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970557T>A

Allele/Variant
Source: ss5201251109
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970612G>C

Allele/Variant
Source: ss5201251091
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970737T>C

Allele/Variant
Source: ss5201250935
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968362A>T

Allele/Variant
Source: ss5201251017
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968560A>C

Allele/Variant
Source: ss5201251087
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970481T>C

Allele/Variant
Source: ss5201251048
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970594T>A

sa41204

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-7254
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5201251112
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24969064T>C

Allele/Variant
Source: ss5201251027
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24969490G>T

Allele/Variant
Source: ss5201250954
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968650A>G

Allele/Variant
Source: ss5201251062
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970465A>T

Allele/Variant
Source: ss5201251074
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970580A>T

Allele/Variant
Source: ss5201251024
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970703C>T

Allele/Variant
Source: ss5201251120
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970745G>T

Allele/Variant
Source: ss5201250938
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968770A>G

Allele/Variant
Source: ss5201250977
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968857A>G

Allele/Variant
Source: ss5201251086
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970629G>C

Allele/Variant
Source: ss5201251084
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970684A>T

Allele/Variant
Source: ss5201251026
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24969070T>A

Allele/Variant
Source: ss5201251050
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970326C>T

Allele/Variant
Source: ss5201251040
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970776C>T

Allele/Variant
Source: ss5201251016
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968908C>T

Allele/Variant
Source: ss5201251078
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970068A>T

Allele/Variant
Source: ss5201251046
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970070T>G

Allele/Variant
Source: ss5201251057
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970117T>G

Allele/Variant
Source: ss5201251092
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970071T>G

Allele/Variant
Source: ss5201251067
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970619T>A

Allele/Variant
Source: ss5201251080
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970652T>A

Allele/Variant
Source: ss5201250939
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968896C>T

Allele/Variant
Source: ss5201250945
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968914T>A

Allele/Variant
Source: ss5201250982
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24968342C>T

Allele/Variant
Source: ss5201251063
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970122A>C

Allele/Variant
Source: ss5201251083
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970541G>A

Allele/Variant
Source: ss5201251114
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970563C>G

Allele/Variant
Source: ss5201251043
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970045T>C

Allele/Variant
Source: ss5201251097
Genes: hspa1b (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)8:24970338T>G