90 results for lrrc73
Allele/Variant
Source: rs229305899
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567043G>A

Allele/Variant
Source: rs107718470
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567046C>A

Allele/Variant
Source: rs232865947
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567273C>T

Allele/Variant
Source: rs227372536
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564871G>A

Allele/Variant
Source: rs108650170
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567301A>G

Allele/Variant
Source: rs232550053
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565936C>T

Allele/Variant
Source: rs108170800
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566724C>A

Allele/Variant
Source: rs246295707
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566801C>T

(mRatBN7.2)9:14726349G>A

(Rattus norvegicus)
Allele/Variant
Source: rs8171587
Genes: Lrrc73 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:14726349G>A

(mRatBN7.2)9:14730052A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3321564600
Genes: Lrrc73 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)9:14730052A>C

Allele/Variant
Source: rs241569024
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567630C>T

Allele/Variant
Source: rs107951646
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567980T>C

Allele/Variant
Source: rs221809837
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566240A>C

Allele/Variant
Source: rs107932420
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567678A>G

Allele/Variant
Source: rs244135796
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567715G>A

Allele/Variant
Source: rs107946865
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567259T>C

Allele/Variant
Source: rs580089682
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564520C>T

Allele/Variant
Source: rs229584430
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564728C>A

Allele/Variant
Source: rs108170800
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566724C>T

Allele/Variant
Source: rs221411304
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566920G>A

Allele/Variant
Source: rs221930397
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566640C>T

Allele/Variant
Source: rs262954125
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566842C>A

Allele/Variant
Source: rs586997346
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567306G>C

Allele/Variant
Source: rs255239870
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567427C>T

Allele/Variant
Source: rs247336445
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564902C>T

Allele/Variant
Source: rs228148631
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566497T>C

Allele/Variant
Source: rs584236740
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566786C>T

Allele/Variant
Source: rs265395492
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564768C>G

Allele/Variant
Source: rs587328331
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564558A>T

Allele/Variant
Source: rs261699989
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564638A>C

Allele/Variant
Source: rs236442081
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567553G>C

Allele/Variant
Source: rs211893153
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565003C>T

Allele/Variant
Source: rs237116022
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565013G>A

Allele/Variant
Source: rs240039098
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46566495G>A

Allele/Variant
Source: rs241814175
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564597G>C

Allele/Variant
Source: rs243543880
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564741T>C

Allele/Variant
Source: rs220835534
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567493G>A

Allele/Variant
Source: rs260015235
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46564969C>T

Allele/Variant
Source: rs237116022
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46565013G>C

Allele/Variant
Source: rs107718470
Genes: Lrrc73 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCm39)17:46567046C>G