27 results
Allele/Variant Genes: fgg (Dre) Molecular Consequence: non coding transcript variant
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: 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: 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: 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: ss5199523497
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673987G>A

Allele/Variant
Source: ss5199523438
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)1:25675953C>T

Allele/Variant
Source: ss5199523436
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672937A>G

Allele/Variant
Source: ss5199523470
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675346A>T

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: ss5199523461
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25672926A>T

Allele/Variant
Source: ss5199523458
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673684A>G

Allele/Variant
Source: ss5199523473
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25673875A>G

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: 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: ss5199523494
Genes: fgg (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:25675668A>C