Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TP53 (Hsa) Molecular Consequence: non coding transcript exon variant
(GRCh38)17:7667874G>C
(Homo sapiens)Allele/Variant
Source: rs1049800949
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7667874G>C
(GRCh38)17:7675040C>T
(Homo sapiens)Allele/Variant
Source: rs56226808
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675040C>T
(GRCh38)17:7675044G>C
(Homo sapiens)Allele/Variant
Source: rs1224204682
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675044G>C
(GRCh38)17:7675045C>T
(Homo sapiens)Allele/Variant
Source: rs775915220
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675045C>T
(GRCh38)17:7675047G>T
(Homo sapiens)Allele/Variant
Source: rs370546196
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675047G>T
(GRCh38)17:7674973T>G
(Homo sapiens)Allele/Variant
Source: rs1427441061
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674973T>G
(GRCh38)17:7674985G>T
(Homo sapiens)Allele/Variant
Source: rs1567552335
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674985G>T
(GRCh38)17:7675034T>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7675034T>A
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675034T>A
(GRCh38)17:7667899A>C
(Homo sapiens)Allele/Variant
Source: rs886596112
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7667899A>C
(GRCh38)17:7674295G>C
(Homo sapiens)Allele/Variant
Source: rs876658684
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674295G>C
(GRCh38)17:7668195G>A
(Homo sapiens)Allele/Variant
Source: rs781520227
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7668195G>A
(GRCh38)17:7670601T>C
(Homo sapiens)Allele/Variant
Source: rs878854062
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670601T>C
(GRCh38)17:7670605T>A
(Homo sapiens)Allele/Variant
Source: rs2150993595
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670605T>A
(GRCh38)17:7670589A>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7670589A>G
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670589A>G
(GRCh38)17:7670607A>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7670607A>G
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670607A>G
(GRCh38)17:7674972C>G
(Homo sapiens)Allele/Variant
Source: rs1202793339
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674972C>G
(GRCh38)17:7674987G>A
(Homo sapiens)Allele/Variant
Source: rs2151028724
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674987G>A
(GRCh38)17:7675244A>C
(Homo sapiens)Allele/Variant
Source: rs1460362518
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675244A>C
(GRCh38)17:7676277A>C
(Homo sapiens)Allele/Variant
Source: rs768373702
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676277A>C
(GRCh38)17:7670604C>G
(Homo sapiens)Allele/Variant
Source: rs889930337
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670604C>G
(GRCh38)17:7668194C>T
(Homo sapiens)Allele/Variant
Source: rs1056550417
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7668194C>T
(GRCh38)17:7674293A>G
(Homo sapiens)Allele/Variant
Source: rs1214646363
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674293A>G
(GRCh38)17:7674979C>A
(Homo sapiens)Allele/Variant
Source: rs373797299
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674979C>A
(GRCh38)17:7667923T>G
(Homo sapiens)Allele/Variant
Source: rs2072741680
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7667923T>G
(GRCh38)17:7667908C>A
(Homo sapiens)Allele/Variant
Source: rs183153328
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7667908C>A
(GRCh38)17:7674174T>A
(Homo sapiens)Allele/Variant
Source: rs2151019726
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674174T>A
(GRCh38)17:7676281G>A
(Homo sapiens)Allele/Variant
Source: rs202217267
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676281G>A
(GRCh38)17:7676367A>G
(Homo sapiens)Allele/Variant
Source: rs200053580
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676367A>G
(GRCh38)17:7675978C>A
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7675978C>A
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675978C>A
(GRCh38)17:7666228C>G
(Homo sapiens)Allele/Variant
Source: rs144366923
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7666228C>G
(GRCh38)17:7674972C>T
(Homo sapiens)Allele/Variant
Source: rs1202793339
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_acceptor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674972C>T
(GRCh38)17:7674979C>G
(Homo sapiens)Allele/Variant
Source: rs373797299
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674979C>G
(GRCh38)17:7674982T>C
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7674982T>C
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674982T>C
(GRCh38)17:7674989G>A
(Homo sapiens)Allele/Variant
Source: rs1189939264
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674989G>A
(GRCh38)17:7675033C>T
(Homo sapiens)Allele/Variant
Source: rs547244762
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675033C>T
(GRCh38)17:7675048C>T
(Homo sapiens)Allele/Variant
Source: rs1555525956
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675048C>T
(GRCh38)17:7670607A>T
(Homo sapiens)Allele/Variant
Source: rs2150993637
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670607A>T
(GRCh38)17:7669911C>T
(Homo sapiens)Allele/Variant
Source: rs6503048
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7669911C>T
(GRCh38)17:7673847A>C
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7673847A>C
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673847A>C
(GRCh38)17:7674977A>G
(Homo sapiens)Allele/Variant
Source: rs1555525929
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674977A>G
(GRCh38)17:7675036C>T
(Homo sapiens)Allele/Variant
Source: rs2151029448
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675036C>T
(GRCh38)17:7675990T>C
(Homo sapiens)Allele/Variant
Source: rs1060501192
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675990T>C
(GRCh38)17:7667901C>T
(Homo sapiens)Allele/Variant
Source: rs2072740794
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7667901C>T
(GRCh38)17:7675242G>C
(Homo sapiens)Allele/Variant
Source: rs2151034268
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675242G>C
(GRCh38)17:7676277A>G
(Homo sapiens)Allele/Variant
Source: rs768373702
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676277A>G
(GRCh38)17:7669703G>A
(Homo sapiens)Allele/Variant
Source: rs897689379
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7669703G>A
(GRCh38)17:7673686G>A
(Homo sapiens)Allele/Variant
Source: rs1057523528
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673686G>A
(GRCh38)17:7673303C>G
(Homo sapiens)Allele/Variant
Source: rs1470589675
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673303C>G
(GRCh38)17:7673312A>C
(Homo sapiens)Allele/Variant
Source: rs3021068
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673312A>C
(GRCh38)17:7673312A>G
(Homo sapiens)Allele/Variant
Source: rs3021068
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673312A>G