1,819 results
Allele/Variant Genes: Unc5b (Mmu)

Unc5bem1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7576577
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5btm1Dyl

(Mus musculus)
Allele/Variant
Source: MGI:5774844
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5bem1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7587422
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5bGt(OST451292)Lex

(Mus musculus)
Allele/Variant
Source: MGI:5085883
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: MGI:6849725
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5btm1.1Dyl

(Mus musculus)
Allele/Variant
Source: MGI:3654305
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5btm1.1Slac

(Mus musculus)
Allele/Variant
Source: MGI:7338938
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5bem2Cya

(Mus musculus)
Allele/Variant
Source: MGI:7587423
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5bem2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7308257
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Unc5btm1Matl

(Mus musculus)
Allele/Variant
Source: MGI:3760978
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs47022998
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60598467A>G

Allele/Variant
Source: rs224802316
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60598642A>G

Allele/Variant
Source: rs236194900
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60598692A>G

Allele/Variant
Source: rs220368730
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60598925C>T

Allele/Variant
Source: rs223182509
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600675A>G

Allele/Variant
Source: rs223927960
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600896A>G

Allele/Variant
Source: rs220294471
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600127A>G

Allele/Variant
Source: rs218739254
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600522T>C

Allele/Variant
Source: rs265287810
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602614A>G

Allele/Variant
Source: rs223633336
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602019C>T

Allele/Variant
Source: rs244011556
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60601305C>G

Allele/Variant
Source: rs218643093
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60601550C>T

Allele/Variant
Source: rs580868118
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60603947C>T

Allele/Variant
Source: rs236698962
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60603970G>A

Allele/Variant
Source: rs262296594
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60604035G>A

Allele/Variant
Source: rs250025936
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60604281G>A

Allele/Variant
Source: rs224097026
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60604861T>C

Allele/Variant
Source: rs251102948
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60605652A>G

Allele/Variant
Source: rs241597889
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60607201T>C

Allele/Variant
Source: rs1134413561
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60612180C>T

Allele/Variant
Source: rs255190513
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60599327C>T

Allele/Variant
Source: rs237109292
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60599545G>A

Allele/Variant
Source: rs249759157
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60599595C>T

Allele/Variant
Source: rs259999395
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602464G>C

Allele/Variant
Source: rs218234774
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602950C>A

Allele/Variant
Source: rs50991291
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60601819G>A

Allele/Variant
Source: rs247561655
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602040T>C

Allele/Variant
Source: rs218196192
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602088T>C

Allele/Variant
Source: rs50678748
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602103G>T

Allele/Variant
Source: rs579487146
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60602191C>T

Allele/Variant
Source: rs252194254
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60601175T>A

Allele/Variant
Source: rs250412785
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600001G>A

Allele/Variant
Source: rs241557830
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60601561G>A

Allele/Variant
Source: rs215979459
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60600242T>C

Allele/Variant
Source: rs212879445
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60599305C>T

Allele/Variant
Source: rs259647064
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60599464C>T

Allele/Variant
Source: rs244581459
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60603069A>C

Allele/Variant
Source: rs232535558
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60603617G>T

Allele/Variant
Source: rs225870655
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60604433G>A

Allele/Variant
Source: rs244990118
Genes: Unc5b (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)10:60606794C>G