322 results
Allele/Variant Genes: scyl2 (Dre)

uab409

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-220720-26
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5200418398
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26060274T>A

Allele/Variant
Source: ss5200418355
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26062533G>T

Allele/Variant
Source: ss5200418745
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081911C>A

Allele/Variant
Source: ss5200418624
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26076387C>A

Allele/Variant
Source: ss5200418633
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26078412A>C

Allele/Variant
Source: ss5200418702
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26079116T>C

Allele/Variant
Source: ss5200418661
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26079721T>A

Allele/Variant
Source: ss5200418701
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081176A>T

Allele/Variant
Source: ss5200418655
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081248A>T

Allele/Variant
Source: ss5200418611
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081561C>T

Allele/Variant
Source: ss5200418317
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26059604A>G

Allele/Variant
Source: ss5200418368
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26059785A>G

Allele/Variant
Source: ss5200418406
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26060390A>G

Allele/Variant
Source: ss5200418334
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26060437T>A

Allele/Variant
Source: ss5200418428
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26065415T>C

Allele/Variant
Source: ss5200418700
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081629C>G

Allele/Variant
Source: ss5200418426
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26065566A>T

Allele/Variant
Source: ss5200418430
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26067220T>C

Allele/Variant
Source: ss5200418479
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26068484G>A

Allele/Variant
Source: ss5200418419
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069588T>G

sa20293

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15226
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: Not Available

sa20292

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-131217-15225
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: ss5200418653
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26078410T>C

Allele/Variant
Source: ss5200418694
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26079446C>A

Allele/Variant
Source: ss5200418486
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26064788G>T

Allele/Variant
Source: ss5200418418
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26065462G>A

Allele/Variant
Source: ss5200418445
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26067710G>T

Allele/Variant
Source: ss5200418450
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069451T>C

Allele/Variant
Source: ss5200418554
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26071385T>A

Allele/Variant
Source: ss5200418561
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072385C>G

Allele/Variant
Source: ss5200418524
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072722G>A

Allele/Variant
Source: ss5200418541
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26073373A>T

Allele/Variant
Source: ss5200418625
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26078084G>A

Allele/Variant
Source: ss5200418619
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26078847A>G

Allele/Variant
Source: ss5200418637
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26079267T>G

Allele/Variant
Source: ss5200418500
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26064594A>G

Allele/Variant
Source: ss5200418465
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26065606A>T

Allele/Variant
Source: ss5200418467
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26067204A>G

Allele/Variant
Source: ss5200418466
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26067232C>A

Allele/Variant
Source: ss5200418483
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26067780G>T

Allele/Variant
Source: ss5200418433
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069177G>A

Allele/Variant
Source: ss5200418544
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26073397A>T

Allele/Variant
Source: ss5200418681
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081588T>C

Allele/Variant
Source: ss5200418697
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081635C>G

Allele/Variant
Source: ss5200418689
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26081656A>G

Allele/Variant
Source: ss5200418421
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069013C>T

Allele/Variant
Source: ss5200418636
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26079993C>T

Allele/Variant
Source: ss5200418443
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26068438A>G

Allele/Variant
Source: ss5200418498
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26068528A>G