Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: E2F1 (Hsa)
(GRCh38)20:33686083G>C
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.33686083G>C
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686083G>C
(GRCh38)20:33676807G>A
(Homo sapiens)Allele/Variant
Source: rs535111025
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676807G>A
(GRCh38)20:33676869C>T
(Homo sapiens)Allele/Variant
Source: rs3213176
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676869C>T
(GRCh38)20:33676801G>A
(Homo sapiens)Allele/Variant
Source: rs147013405
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676801G>A
(GRCh38)20:33686039G>A
(Homo sapiens)Allele/Variant
Source: rs907590073
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686039G>A
(GRCh38)20:33686231A>T
(Homo sapiens)Allele/Variant
Source: rs574523664
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686231A>T
(GRCh38)20:33676901G>A
(Homo sapiens)Allele/Variant
Source: rs773280034
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676901G>A
(GRCh38)20:33676909C>T
(Homo sapiens)Allele/Variant
Source: rs201607111
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676909C>T
(GRCh38)20:33686034A>C
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.33686034A>C
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686034A>C
(GRCh38)20:33686154G>A
(Homo sapiens)Allele/Variant
Source: rs3213143
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686154G>A
(GRCh38)20:33686204C>G
(Homo sapiens)Allele/Variant
Source: rs1019744956
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686204C>G
(GRCh38)20:33677143G>A
(Homo sapiens)Allele/Variant
Source: rs564825532
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33677143G>A
(GRCh38)20:33678328C>T
(Homo sapiens)Allele/Variant
Source: rs35385772
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33678328C>T
(GRCh38)20:33676859G>C
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.33676859G>C
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676859G>C
(GRCh38)20:33676727C>A
(Homo sapiens)Allele/Variant
Source: rs3213177
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676727C>A
(GRCh38)20:33676870G>A
(Homo sapiens)Allele/Variant
Source: rs142009843
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676870G>A
(GRCh38)20:33677440C>T
(Homo sapiens)Allele/Variant
Source: rs3213173
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33677440C>T
(GRCh38)20:33677525C>T
(Homo sapiens)Allele/Variant
Source: rs35807460
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33677525C>T
(GRCh38)20:33679830C>T
(Homo sapiens)Allele/Variant
Source: rs864622017
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33679830C>T
(GRCh38)20:33685994G>A
(Homo sapiens)Allele/Variant
Source: rs534919188
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33685994G>A
(GRCh38)20:33686031C>G
(Homo sapiens)Allele/Variant
Source: rs984482701
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686031C>G
(GRCh38)20:33686033C>A
(Homo sapiens)Allele/Variant
Source: rs1306675586
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686033C>A
(GRCh38)20:33677441G>A
(Homo sapiens)Allele/Variant
Source: rs529768589
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33677441G>A
(GRCh38)20:33686118G>C
(Homo sapiens)Allele/Variant
Source: rs751858610
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686118G>C
(GRCh38)20:33676905C>T
(Homo sapiens)Allele/Variant
Source: rs1453160857
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33676905C>T
(GRCh38)20:33677154G>A
(Homo sapiens)Allele/Variant
Source: rs138360482
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33677154G>A
(GRCh38)20:33680374C>T
(Homo sapiens)Allele/Variant
Source: rs145741678
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33680374C>T
(GRCh38)20:33686066C>G
(Homo sapiens)Allele/Variant
Source: NC_000020.11:g.33686066C>G
Genes: E2F1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)20:33686066C>G