Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CPSF6 (Hsa)
(GRCh38)12:69253132C>T
(Homo sapiens)Allele/Variant
Source: rs1227467387
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69253132C>T
(GRCh38)12:69258872G>A
(Homo sapiens)Allele/Variant
Source: rs1319456781
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258872G>A
(GRCh38)12:69260136A>G
(Homo sapiens)Allele/Variant
Source: rs749608024
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69260136A>G
(GRCh38)12:69262526G>C
(Homo sapiens)Allele/Variant
Source: rs751188299
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69262526G>C
(GRCh38)12:69258811C>G
(Homo sapiens)Allele/Variant
Source: rs939481174
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258811C>G
(GRCh38)12:69257828G>A
(Homo sapiens)Allele/Variant
Source: rs1367649704
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69257828G>A
(GRCh38)12:69257890C>G
(Homo sapiens)Allele/Variant
Source: rs61754516
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69257890C>G
(GRCh38)12:69251179A>G
(Homo sapiens)Allele/Variant
Source: rs1024211546
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69251179A>G
(GRCh38)12:69256788G>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.69256788G>A
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69256788G>A
(GRCh38)12:69258709C>T
(Homo sapiens)Allele/Variant
Source: rs1248836755
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258709C>T
(GRCh38)12:69258881G>C
(Homo sapiens)Allele/Variant
Source: rs1272594701
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258881G>C
(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
(GRCh38)12:69253081G>A
(Homo sapiens)Allele/Variant
Source: rs150030798
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69253081G>A
(GRCh38)12:69259042C>G
(Homo sapiens)Allele/Variant
Source: rs867013321
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69259042C>G
(GRCh38)12:69258860C>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.69258860C>T
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258860C>T
(GRCh38)12:69259091G>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.69259091G>A
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69259091G>A
(GRCh38)12:69258757C>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.69258757C>T
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69258757C>T
(GRCh38)12:69257896C>T
(Homo sapiens)Allele/Variant
Source: rs755647632
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69257896C>T
(GRCh38)12:69257848G>A
(Homo sapiens)Allele/Variant
Source: rs200906163
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69257848G>A
(GRCh38)12:69262457C>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.69262457C>A
Genes: CPSF6 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:69262457C>A