Version: 8.0.0
Date: Tue Jan 28 2025
1 results
Allele/Variant Genes: CPSF6 (Hsa) Molecular Consequence: synonymous variant

(GRCh38)12:69262539C>T

(Homo sapiens)
Allele/Variant
Source: rs1438062658
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69262539C>T