Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: E2F5-DT (Hsa)
(GRCh38)8:85135901A>G
(Homo sapiens)Allele/Variant
Source: rs773183506
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85135901A>G
(GRCh38)8:85109592T>C
(Homo sapiens)Allele/Variant
Source: rs758221070
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109592T>C
(GRCh38)8:85109759G>A
(Homo sapiens)Allele/Variant
Source: rs62525422
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109759G>A
(GRCh38)8:85113066G>T
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85113066G>T
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85113066G>T
(GRCh38)8:85123447A>G
(Homo sapiens)Allele/Variant
Source: rs374888725
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85123447A>G
(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)8:85135776T>G
(Homo sapiens)Allele/Variant
Source: rs76410993
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85135776T>G
(GRCh38)8:85124809A>G
(Homo sapiens)Allele/Variant
Source: rs751998365
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85124809A>G
(GRCh38)8:85113072G>T
(Homo sapiens)Allele/Variant
Source: rs772964315
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85113072G>T
(GRCh38)8:85113091G>A
(Homo sapiens)Allele/Variant
Source: rs76773098
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85113091G>A
(GRCh38)8:85135870G>A
(Homo sapiens)Allele/Variant
Source: rs780329669
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85135870G>A
(GRCh38)8:85135892C>A
(Homo sapiens)Allele/Variant
Source: rs748142470
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85135892C>A
(GRCh38)8:85124888G>T
(Homo sapiens)Allele/Variant
Source: rs1809851098
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85124888G>T
(GRCh38)8:85115377C>T
(Homo sapiens)Allele/Variant
Source: rs267602020
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85115377C>T
(GRCh38)8:85115431A>G
(Homo sapiens)Allele/Variant
Source: rs768325015
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85115431A>G
(GRCh38)8:85138208G>A
(Homo sapiens)Allele/Variant
Source: rs371922118
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85138208G>A
(GRCh38)8:85115183A>G
(Homo sapiens)Allele/Variant
Source: rs3736038
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85115183A>G
(GRCh38)8:85115427T>C
(Homo sapiens)Allele/Variant
Source: rs1413963324
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85115427T>C
(GRCh38)8:85134911C>T
(Homo sapiens)Allele/Variant
Source: rs201585531
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85134911C>T
(GRCh38)8:85138042A>G
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85138042A>G
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85138042A>G
(GRCh38)8:85130013C>T
(Homo sapiens)Allele/Variant
Source: rs765839225
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85130013C>T
(GRCh38)8:85131832A>C
(Homo sapiens)Allele/Variant
Source: rs6985225
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85131832A>C
(GRCh38)8:85134857G>C
(Homo sapiens)Allele/Variant
Source: rs1323983535
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85134857G>C
(GRCh38)8:85109629G>T
(Homo sapiens)Allele/Variant
Source: rs374046471
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109629G>T
(GRCh38)8:85109678A>G
(Homo sapiens)Allele/Variant
Source: rs200588342
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109678A>G
(GRCh38)8:85109742C>G
(Homo sapiens)Allele/Variant
Source: rs993305590
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109742C>G
(GRCh38)8:85138348C>T
(Homo sapiens)Allele/Variant
Source: rs74339310
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85138348C>T
(GRCh38)8:85135954G>T
(Homo sapiens)Allele/Variant
Source: rs532088365
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85135954G>T
(GRCh38)8:85141382G>A
(Homo sapiens)Allele/Variant
Source: rs201637203
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85141382G>A
(GRCh38)8:85126800G>C
(Homo sapiens)Allele/Variant
Source: rs1227893635
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85126800G>C
(GRCh38)8:85137496G>A
(Homo sapiens)Allele/Variant
Source: rs190022501
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85137496G>A
(GRCh38)8:85138143G>A
(Homo sapiens)Allele/Variant
Source: rs762316787
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85138143G>A
(GRCh38)8:85115534G>A
(Homo sapiens)Allele/Variant
Source: rs1422485408
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85115534G>A
(GRCh38)8:85129286A>C
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85129286A>C
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85129286A>C
(GRCh38)8:85135947T>A
(Homo sapiens)Allele/Variant
Source: rs1469310133
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85135947T>A
(GRCh38)8:85137614G>C
(Homo sapiens)Allele/Variant
Source: rs1482989472
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85137614G>C
(GRCh38)8:85126761G>C
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85126761G>C
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85126761G>C
(GRCh38)8:85129380G>A
(Homo sapiens)Allele/Variant
Source: rs760613708
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85129380G>A
(GRCh38)8:85138157G>A
(Homo sapiens)Allele/Variant
Source: rs765806932
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85138157G>A
(GRCh38)8:85123434G>A
(Homo sapiens)Allele/Variant
Source: rs370959283
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85123434G>A
(GRCh38)8:85115404A>G
(Homo sapiens)Allele/Variant
Source: rs549511486
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85115404A>G
(GRCh38)8:85131847T>G
(Homo sapiens)Allele/Variant
Source: rs538616734
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85131847T>G
(GRCh38)8:85137474A>G
(Homo sapiens)Allele/Variant
Source: rs574150443
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85137474A>G
(GRCh38)8:85124957A>G
(Homo sapiens)Allele/Variant
Source: rs376182400
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85124957A>G
(GRCh38)8:85126746G>A
(Homo sapiens)Allele/Variant
Source: rs201242609
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85126746G>A
(GRCh38)8:85129325C>T
(Homo sapiens)Allele/Variant
Source: rs375521750
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85129325C>T
(GRCh38)8:85109735G>A
(Homo sapiens)Allele/Variant
Source: NC_000008.11:g.85109735G>A
Genes: E2F5-DT (Hsa), LRRCC1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)8:85109735G>A
(GRCh38)8:85115466C>T
(Homo sapiens)Allele/Variant
Source: rs202212290
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85115466C>T
(GRCh38)8:85107306C>T
(Homo sapiens)Allele/Variant
Source: rs371924871
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85107306C>T
(GRCh38)8:85107362T>A
(Homo sapiens)Allele/Variant
Source: rs774905053
Genes: E2F5-DT (Hsa), LRRCC1 (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)8:85107362T>A