Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: E2F8 (Hsa) Molecular Consequence: missense variant
(GRCh38)11:19238070G>A
(Homo sapiens)Allele/Variant
Source: rs73416784
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19238070G>A
(GRCh38)11:19225862G>A
(Homo sapiens)Allele/Variant
Source: rs796969
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225862G>A
(GRCh38)11:19237944A>G
(Homo sapiens)Allele/Variant
Source: rs12291291
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19237944A>G
(GRCh38)11:19225332G>A
(Homo sapiens)Allele/Variant
Source: rs138183110
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225332G>A
(GRCh38)11:19225551C>T
(Homo sapiens)Allele/Variant
Source: rs3740965
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225551C>T
(GRCh38)11:19234934G>A
(Homo sapiens)Allele/Variant
Source: rs144097514
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234934G>A
(GRCh38)11:19232262G>A
(Homo sapiens)Allele/Variant
Source: rs148702233
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19232262G>A