397 results
Allele/Variant Genes: ostf1 (Dre)
Allele/Variant
Source: ss5199282174
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732037T>C

Allele/Variant
Source: ss5199282154
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732043T>G

Allele/Variant
Source: ss5199282133
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732190A>T

Allele/Variant
Source: ss5199282193
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732191A>C

Allele/Variant
Source: ss5199282123
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733321C>T

Allele/Variant
Source: ss5199282233
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6738448A>G

Allele/Variant
Source: ss5199282258
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6739108G>A

Allele/Variant
Source: ss5199282187
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733037A>T

Allele/Variant
Source: ss5199282212
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732485T>C

Allele/Variant
Source: ss5199282386
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6742197G>A

Allele/Variant
Source: ss5199282246
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6736154A>G

Allele/Variant
Source: ss5199282476
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743709G>A

Allele/Variant
Source: ss5199282450
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6744511T>A

Allele/Variant
Source: ss5199282276
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6736469T>A

Allele/Variant
Source: ss5199282282
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6735000G>A

Allele/Variant
Source: ss5199282468
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743439C>G

Allele/Variant
Source: ss5199282250
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733650T>C

Allele/Variant
Source: ss5199282256
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733660C>A

Allele/Variant
Source: ss5199282428
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743835T>C

Allele/Variant
Source: ss5199282483
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743409A>T

Allele/Variant
Source: ss5199282218
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6736704C>T

Allele/Variant
Source: ss5199282290
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6736847T>C

Allele/Variant
Source: ss5199282374
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6741972T>G

Allele/Variant
Source: ss5199282345
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6742793T>A

Allele/Variant
Source: ss5199282078
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6726473T>C

Allele/Variant
Source: ss5199282051
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6727407G>A

Allele/Variant
Source: ss5199282364
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6741463A>G

Allele/Variant
Source: ss5199282501
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743303A>C

Allele/Variant
Source: ss5199282242
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733548A>G

Allele/Variant
Source: ss5199282465
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743836G>A

Allele/Variant
Source: ss5199282162
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732013G>A

Allele/Variant
Source: ss5199282135
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733487T>C

Allele/Variant
Source: ss5199282371
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6739928G>T

Allele/Variant
Source: ss5199282217
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6738379G>T

Allele/Variant
Source: ss5199282113
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6731058T>A

Allele/Variant
Source: ss5199282091
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6731293A>T

Allele/Variant
Source: ss5199282049
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6731466T>G

Allele/Variant
Source: ss5199282166
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732662A>G

Allele/Variant
Source: ss5199282183
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6732028T>C

Allele/Variant
Source: ss5199282189
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733415T>C

Allele/Variant
Source: ss5199282298
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6736530A>G

Allele/Variant
Source: ss5199282437
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743334A>T

Allele/Variant
Source: ss5199282515
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743652T>C

Allele/Variant
Source: ss5199282438
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6743653A>G

Allele/Variant
Source: ss5199282143
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733358G>A

Allele/Variant
Source: ss5199282127
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733414A>G

Allele/Variant
Source: ss5199282139
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6733528C>T

Allele/Variant
Source: ss5199282054
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6730944A>T

Allele/Variant
Source: ss5199282116
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6731441C>T

Allele/Variant
Source: ss5199282094
Genes: ostf1 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCz11)5:6727232G>A