9 results
Allele/Variant Genes: Cd24a (Mmu) Molecular Consequence: non coding transcript exon variant
Allele/Variant
Source: rs224125246
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454763C>G

Allele/Variant
Source: rs229208826
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454666C>T

Allele/Variant
Source: rs216313077
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43455186G>A

Allele/Variant
Source: rs212838003
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454719T>A

Allele/Variant
Source: rs8244386
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454475C>G

Allele/Variant
Source: rs265407151
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454587G>A

Allele/Variant
Source: rs245979568
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454561C>T

Allele/Variant
Source: rs248033472
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43454691G>A

Allele/Variant
Source: rs235251824
Genes: Cd24a (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCm39)10:43455190T>C