1,012 results
Allele/Variant Genes: Lratd2 (Mmu)

Lratd2em1(IMPC)Ccpcz

(Mus musculus)
Allele/Variant
Source: MGI:6316150
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available

Allele/Variant
Source: rs864300550
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60691243A>T

Allele/Variant
Source: rs261654459
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60697356A>G

Allele/Variant
Source: rs51960387
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60691512A>T

Allele/Variant
Source: rs255349664
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698515G>A

Allele/Variant
Source: rs584560845
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698540A>T

Allele/Variant
Source: rs214885927
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698725G>A

Allele/Variant
Source: rs46499452
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698793T>C

Allele/Variant
Source: rs45670891
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60692727G>A

Allele/Variant
Source: rs45634837
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60699749T>A

Allele/Variant
Source: rs248867955
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693178C>T

Allele/Variant
Source: rs1134181607
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60691513A>T

Allele/Variant
Source: rs47129003
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60696594A>C

Allele/Variant
Source: rs231586192
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693166G>A

Allele/Variant
Source: rs264902766
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693324C>A

Allele/Variant
Source: rs239154241
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693337G>A

Allele/Variant
Source: rs581020560
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60697725C>G

Allele/Variant
Source: rs578816221
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698626A>G

Allele/Variant
Source: rs32459407
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700421T>G

Allele/Variant
Source: rs239290423
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700627T>A

Allele/Variant
Source: rs213489540
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60701133C>T

Allele/Variant
Source: rs247798952
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60696297A>C

Allele/Variant
Source: rs221661114
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60697644T>C

Allele/Variant
Source: rs236701055
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60691589G>A

Allele/Variant
Source: rs586633498
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60692869C>T

Allele/Variant
Source: rs262657416
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698890G>A

Allele/Variant
Source: rs260394070
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693012G>T

Allele/Variant
Source: rs247267084
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693351G>A

Allele/Variant
Source: rs221237520
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693511C>G

Allele/Variant
Source: rs221134832
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693612G>A

Allele/Variant
Source: rs253457907
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693792A>C

Allele/Variant
Source: rs247324454
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60690906G>A

Allele/Variant
Source: rs225435606
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60691061A>G

Allele/Variant
Source: rs264968175
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60694832C>G

Allele/Variant
Source: rs13462780
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60696580A>C

Allele/Variant
Source: rs51037161
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60698925C>T

Allele/Variant
Source: rs48419729
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60699001T>C

Allele/Variant
Source: rs223232190
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60699006G>A

Allele/Variant
Source: rs256564869
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700301G>C

Allele/Variant
Source: rs231068576
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700329C>A

Allele/Variant
Source: rs217143821
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700357G>T

Allele/Variant
Source: rs212804966
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693291C>T

Allele/Variant
Source: rs242046689
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693574C>A

Allele/Variant
Source: rs236772365
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700088G>A

Allele/Variant
Source: rs579163826
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700224G>A

Allele/Variant
Source: rs265133008
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60693687T>G

Allele/Variant
Source: rs579498880
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60708040C>T

Allele/Variant
Source: rs259178638
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60708045T>C

Allele/Variant
Source: rs240848518
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60700544T>G

Allele/Variant
Source: rs246895987
Genes: Lratd2 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)15:60708249A>G