Version: 8.0.0
Date: Tue Jan 28 2025
11 results
Allele/Variant Genes: E2F1 (Hsa) Molecular Consequence: missense variant

(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)20:33676801G>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)20:33676909C>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)20:33686154G>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)20:33676727C>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)20:33685994G>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)20:33677441G>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)20:33677154G>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