Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: E2F5 (Hsa)
(GRCh38)8:85177559G>A
(Homo sapiens)Allele/Variant
Source: rs749449900
Genes: E2F5 (Hsa), E2F5-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85177559G>A
(GRCh38)8:85207448G>T
(Homo sapiens)Allele/Variant
Source: rs1386552061
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85207448G>T
(GRCh38)8:85177631G>A
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85177631G>A
Genes: E2F5 (Hsa), E2F5-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85177631G>A
(GRCh38)8:85177653C>A
(Homo sapiens)Allele/Variant
Source: rs374657776
Genes: E2F5 (Hsa), E2F5-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85177653C>A
(GRCh38)8:85209147G>C
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85209147G>C
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85209147G>C
(GRCh38)8:85209220G>C
(Homo sapiens)Allele/Variant
Source: rs747579309
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85209220G>C
(GRCh38)8:85213795A>T
(Homo sapiens)Allele/Variant
Source: rs779834479
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85213795A>T
(GRCh38)8:85202155T>A
(Homo sapiens)Allele/Variant
Source: rs1272861020
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85202155T>A
(GRCh38)8:85206219T>A
(Homo sapiens)Allele/Variant
Source: rs202172071
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85206219T>A
(GRCh38)8:85209379C>A
(Homo sapiens)Allele/Variant
Source: rs1431907802
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85209379C>A
(GRCh38)8:85209353A>C
(Homo sapiens)Allele/Variant
Source: rs1425657246
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85209353A>C
(GRCh38)8:85203130A>G
(Homo sapiens)Allele/Variant
Source: rs1563981708
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85203130A>G
(GRCh38)8:85206201C>A
(Homo sapiens)Allele/Variant
Source: rs749670424
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85206201C>A
(GRCh38)8:85177512A>G
(Homo sapiens)Allele/Variant
Source: rs1812108556
Genes: E2F5 (Hsa), E2F5-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85177512A>G
(GRCh38)8:85212176T>A
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85212176T>A
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85212176T>A
(GRCh38)8:85177544G>A
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85177544G>A
Genes: E2F5 (Hsa), E2F5-DT (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85177544G>A
(GRCh38)8:85203219G>A
(Homo sapiens)Allele/Variant
Source: rs763392575
Genes: E2F5 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85203219G>A