Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TP53 (Hsa) Molecular Consequence: missense 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)17:7674824C>A
(Homo sapiens)Allele/Variant
Source: rs587778001
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674824C>A
(GRCh38)17:7674828T>C
(Homo sapiens)Allele/Variant
Source: rs34949160
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674828T>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)17:7675063T>G
(Homo sapiens)Allele/Variant
Source: rs1597369559
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675063T>G
(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)17:7675219G>A
(Homo sapiens)Allele/Variant
Source: rs769270327
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675219G>A
(GRCh38)17:7676185C>A
(Homo sapiens)Allele/Variant
Source: rs1567556752
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)17:7676185C>A
(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)17:7674856G>A
(Homo sapiens)Allele/Variant
Source: rs2151025685
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674856G>A
(GRCh38)17:7676218C>A
(Homo sapiens)Allele/Variant
Source: rs1567556930
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)17:7676218C>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)17:7673598G>A
(Homo sapiens)Allele/Variant
Source: rs876660829
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673598G>A
(GRCh38)17:7674246G>A
(Homo sapiens)Allele/Variant
Source: rs1057522275
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674246G>A
(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)17:7668194C>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)17:7673792G>A
(Homo sapiens)Allele/Variant
Source: rs2151016064
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673792G>A
(GRCh38)17:7674249A>T
(Homo sapiens)Allele/Variant
Source: rs193920789
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)17:7674249A>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)17:7675198G>A
(Homo sapiens)Allele/Variant
Source: rs1555526254
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675198G>A
(GRCh38)17:7675069G>A
(Homo sapiens)Allele/Variant
Source: rs876659582
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675069G>A
(GRCh38)17:7676189T>G
(Homo sapiens)Allele/Variant
Source: rs749289195
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676189T>G
(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)17:7669611A>T
(Homo sapiens)Allele/Variant
Source: rs1555524079
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7669611A>T
(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)17:7676565G>A
(Homo sapiens)Allele/Variant
Source: rs568171603
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676565G>A
(GRCh38)17:7668539G>A
(Homo sapiens)Allele/Variant
Source: rs114831472
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7668539G>A
(GRCh38)17:7668783C>T
(Homo sapiens)Allele/Variant
Source: rs17884306
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7668783C>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)17:7676397A>G
(Homo sapiens)Allele/Variant
Source: rs1555526932
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7676397A>G
(GRCh38)17:7670694C>A
(Homo sapiens)Allele/Variant
Source: rs17882252
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670694C>A
(GRCh38)17:7673750G>A
(Homo sapiens)Allele/Variant
Source: rs1555525135
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673750G>A
(GRCh38)17:7673768T>G
(Homo sapiens)Allele/Variant
Source: rs786203004
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673768T>G
(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)17:7674871A>G
(Homo sapiens)Allele/Variant
Source: rs1567551150
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_lost, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674871A>G
(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)17:7673834A>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7673834A>G
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, stop_lost, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673834A>G