Version: 8.0.0
Date: Tue Jan 28 2025
11 results for btg1
Allele/Variant Molecular Consequence: missense variant

(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
Gene Synonyms: BTG1 binding factor 1

(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
Gene Synonyms: BTG1 binding factor 1

(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
Gene Synonyms: BTG1 binding factor 1

(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
Gene Synonyms: BTG1 binding factor 1

(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
Gene Synonyms: BTG1 binding factor 1

(GRCh38)12:92144118G>A

(Homo sapiens)
Allele/Variant
Source: rs1246644859
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144118G>A

(GRCh38)12:92145484C>A

(Homo sapiens)
Allele/Variant
Source: rs1263908473
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145484C>A

(GRCh38)12:92145520T>G

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.92145520T>G
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145520T>G

(GRCh38)12:92144126C>T

(Homo sapiens)
Allele/Variant
Source: NC_000012.12:g.92144126C>T
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144126C>T

(GRCh38)12:92144199T>C

(Homo sapiens)
Allele/Variant
Source: rs375522490
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92144199T>C

(GRCh38)12:92145500T>C

(Homo sapiens)
Allele/Variant
Source: rs2136950034
Genes: BTG1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:92145500T>C