87 results
Allele/Variant Genes: fgg (Dre)

zko488a

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-412
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199523403
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25670030A>C

Allele/Variant
Source: ss5199523413
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673194G>A

Allele/Variant
Source: ss5199523493
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673984T>G

Allele/Variant
Source: ss5199523412
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674030G>C

Allele/Variant
Source: ss5199523451
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675486A>T

Allele/Variant
Source: ss5199523417
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25676561A>C

Allele/Variant
Source: ss5199523487
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25677697T>C

Allele/Variant
Source: ss5199523544
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25678492G>A

Allele/Variant
Source: ss5199523498
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674964A>T

Allele/Variant
Source: ss5199523402
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25671062C>T

sa6585

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-161003-18369
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199523546
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25679077C>A

Allele/Variant
Source: ss5199523469
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25671847C>T

Allele/Variant
Source: ss5199523457
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673254A>G

Allele/Variant
Source: ss5199523431
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673463G>A

Allele/Variant
Source: ss5199523456
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674170A>T

Allele/Variant
Source: ss5199523485
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674863C>A

Allele/Variant
Source: ss5199523490
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675067C>T

Allele/Variant
Source: ss5199523434
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675780G>C

Allele/Variant
Source: ss5199523442
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25676730C>G

Allele/Variant
Source: ss5199523595
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25677871C>T

Allele/Variant
Source: ss5199523510
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25678504C>T

Allele/Variant
Source: ss5199523468
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672002T>A

Allele/Variant
Source: ss5199523480
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672192T>A

Allele/Variant
Source: ss5199523455
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675478T>A

Allele/Variant
Source: ss5199523410
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25676464G>A

Allele/Variant
Source: ss5199523445
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25676473G>A

Allele/Variant
Source: ss5199523424
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25677427C>T

Allele/Variant
Source: ss5199523514
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25679196A>C

Allele/Variant
Source: ss5199523439
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25671256A>T

Allele/Variant
Source: ss5199523416
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672165C>T

Allele/Variant
Source: ss5199523454
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672940A>C

Allele/Variant
Source: ss5199523459
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673562A>G

Allele/Variant
Source: ss5199523475
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674631A>C

Allele/Variant
Source: ss5199523496
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25670272A>C

Allele/Variant
Source: ss5199523415
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672190G>A

Allele/Variant
Source: ss5199523426
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672283T>G

Allele/Variant
Source: ss5199523443
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673218A>G

Allele/Variant
Source: ss5199523471
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673648G>C

Allele/Variant
Source: ss5199523441
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674004A>G

Allele/Variant
Source: ss5199523433
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674053C>T

Allele/Variant
Source: ss5199523421
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25671613T>C

Allele/Variant
Source: ss5199523448
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672054T>C

Allele/Variant
Source: ss5199523488
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672415T>G

Allele/Variant
Source: ss5199523414
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25674355G>A

Allele/Variant
Source: ss5199523430
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25677133T>A

Allele/Variant
Source: ss5199523553
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25678600T>A

Allele/Variant
Source: ss5199523589
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25678952A>T

Allele/Variant
Source: ss5199523571
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25678659G>A