Version: 8.0.0
Date: Tue Jan 28 2025
7 results
Allele/Variant Genes: CNOT7 (Hsa)

(GRCh38)8:17245134C>A

(Homo sapiens)
Allele/Variant
Source: NC_000008.11:g.17245134C>A
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17245134C>A

(GRCh38)8:17243133T>C

(Homo sapiens)
Allele/Variant
Source: rs1810418480
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17243133T>C

(GRCh38)8:17234811G>A

(Homo sapiens)
Allele/Variant
Source: rs771925219
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17234811G>A

(GRCh38)8:17230748T>C

(Homo sapiens)
Allele/Variant
Source: rs1808502366
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17230748T>C

(GRCh38)8:17245139G>A

(Homo sapiens)
Allele/Variant
Source: rs766330962
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17245139G>A

(GRCh38)8:17246679G>A

(Homo sapiens)
Allele/Variant
Source: rs117960717
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17246679G>A

(GRCh38)8:17246633C>G

(Homo sapiens)
Allele/Variant
Source: rs113175413
Genes: CNOT7 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:17246633C>G