10 results
Allele/Variant Genes: mettl14 (Dre)

syu201

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-230418-3
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

zko388b

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-171115-331
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

gyf16

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-210702-8
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199459411
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20067776G>A

Allele/Variant
Source: ss5199459415
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20067612T>A

Allele/Variant
Source: ss5199459372
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20063849G>A

sa12796

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-2480
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5199459462
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20067961A>T

Allele/Variant
Source: ss5199459455
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20068125A>C

Allele/Variant
Source: ss5199459479
Genes: mettl14 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)1:20067610G>A