Version: 8.0.0
Date: Tue Jan 28 2025
1 results
Allele/Variant Genes: CNOT7 (Hsa) Molecular Consequence: non coding transcript variant

(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