232 results
Allele/Variant Genes: scyl2 (Dre) Molecular Consequence: intron variant
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: 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: 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: 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

Allele/Variant
Source: ss5200418468
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26068592G>T

Allele/Variant
Source: ss5200418412
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069203A>T

Allele/Variant
Source: ss5200418416
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26070480T>A

Allele/Variant
Source: ss5200418532
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072017A>C

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: 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

Allele/Variant
Source: ss5200418448
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26070470A>C

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: ss5200418513
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26073470T>A

Allele/Variant
Source: ss5200418566
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26073544A>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: ss5200418594
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26073913G>A

Allele/Variant
Source: ss5200418582
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26074095G>A

Allele/Variant
Source: ss5200418460
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26063604T>A

Allele/Variant
Source: ss5200418516
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072297T>C

Allele/Variant
Source: ss5200418563
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072416C>T

Allele/Variant
Source: ss5200418555
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26072516A>T

Allele/Variant
Source: ss5200418343
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26062122A>G

Allele/Variant
Source: ss5200418350
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26062462C>T

Allele/Variant
Source: ss5200418375
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26062673C>T

Allele/Variant
Source: ss5200418395
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26062717G>T

Allele/Variant
Source: ss5200418461
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26064314A>G

Allele/Variant
Source: ss5200418417
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26064527A>G

Allele/Variant
Source: ss5200418432
Genes: scyl2 (Dre)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCz11)4:26069346G>T