Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: TP53 (Hsa) Molecular Consequence: non coding transcript variant
(GRCh38)17:7670682C>G
(Homo sapiens)Allele/Variant
Source: rs375573770
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670682C>G
(GRCh38)17:7670684C>G
(Homo sapiens)Allele/Variant
Source: rs375338359
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670684C>G
(GRCh38)17:7670693T>A
(Homo sapiens)Allele/Variant
Source: rs1237829645
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670693T>A
(GRCh38)17:7673559C>T
(Homo sapiens)Allele/Variant
Source: rs672601297
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673559C>T
(GRCh38)17:7673565T>C
(Homo sapiens)Allele/Variant
Source: rs2151011521
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673565T>C
(GRCh38)17:7673536T>C
(Homo sapiens)Allele/Variant
Source: rs1064795056
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673536T>C
(GRCh38)17:7673715C>T
(Homo sapiens)Allele/Variant
Source: rs1060501202
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673715C>T
(GRCh38)17:7673723C>A
(Homo sapiens)Allele/Variant
Source: rs2151014201
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673723C>A
(GRCh38)17:7673725G>A
(Homo sapiens)Allele/Variant
Source: rs752701561
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673725G>A
(GRCh38)17:7673799A>G
(Homo sapiens)Allele/Variant
Source: rs1057520006
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673799A>G
(GRCh38)17:7670630C>G
(Homo sapiens)Allele/Variant
Source: rs35993958
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670630C>G
(GRCh38)17:7670637C>T
(Homo sapiens)Allele/Variant
Source: rs587782237
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670637C>T
(GRCh38)17:7670698G>A
(Homo sapiens)Allele/Variant
Source: rs1218459955
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670698G>A
(GRCh38)17:7670700G>A
(Homo sapiens)Allele/Variant
Source: rs587782529
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670700G>A
(GRCh38)17:7670703C>G
(Homo sapiens)Allele/Variant
Source: rs2150995270
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670703C>G
(GRCh38)17:7673578T>C
(Homo sapiens)Allele/Variant
Source: rs1159579789
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673578T>C
(GRCh38)17:7673547A>T
(Homo sapiens)Allele/Variant
Source: rs879254077
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673547A>T
(GRCh38)17:7673564G>C
(Homo sapiens)Allele/Variant
Source: rs863224687
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673564G>C
(GRCh38)17:7673570T>A
(Homo sapiens)Allele/Variant
Source: rs2151011624
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673570T>A
(GRCh38)17:7673714C>T
(Homo sapiens)Allele/Variant
Source: rs2151014014
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673714C>T
(GRCh38)17:7670625T>C
(Homo sapiens)Allele/Variant
Source: rs1287887419
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670625T>C
(GRCh38)17:7670640T>C
(Homo sapiens)Allele/Variant
Source: rs1567541856
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670640T>C
(GRCh38)17:7670620C>T
(Homo sapiens)Allele/Variant
Source: rs1597348743
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670620C>T
(GRCh38)17:7670648T>C
(Homo sapiens)Allele/Variant
Source: rs752142489
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670648T>C
(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)17:7673820C>G
(Homo sapiens)Allele/Variant
Source: rs587780075
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673820C>G
(GRCh38)17:7674193A>C
(Homo sapiens)Allele/Variant
Source: rs28934577
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674193A>C
(GRCh38)17:7673826A>C
(Homo sapiens)Allele/Variant
Source: rs879253942
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673826A>C
(GRCh38)17:7674195T>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7674195T>G
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674195T>G
(GRCh38)17:7674212T>A
(Homo sapiens)Allele/Variant
Source: rs730882007
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674212T>A
(GRCh38)17:7670631C>T
(Homo sapiens)Allele/Variant
Source: rs786203298
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670631C>T
(GRCh38)17:7670645G>A
(Homo sapiens)Allele/Variant
Source: rs1555524382
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670645G>A
(GRCh38)17:7670615T>G
(Homo sapiens)Allele/Variant
Source: NC_000017.11:g.7670615T>G
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7670615T>G
(GRCh38)17:7673592G>C
(Homo sapiens)Allele/Variant
Source: rs1555524991
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673592G>C
(GRCh38)17:7673553T>C
(Homo sapiens)Allele/Variant
Source: rs1245012034
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673553T>C
(GRCh38)17:7673701C>G
(Homo sapiens)Allele/Variant
Source: rs2151013719
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673701C>G
(GRCh38)17:7673535C>A
(Homo sapiens)Allele/Variant
Source: rs11575996
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673535C>A
(GRCh38)17:7673535C>G
(Homo sapiens)Allele/Variant
Source: rs11575996
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673535C>G
(GRCh38)17:7673716C>T
(Homo sapiens)Allele/Variant
Source: rs863224686
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673716C>T
(GRCh38)17:7673726C>T
(Homo sapiens)Allele/Variant
Source: rs756123992
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673726C>T
(GRCh38)17:7673819C>T
(Homo sapiens)Allele/Variant
Source: rs1597362195
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673819C>T
(GRCh38)17:7673776G>A
(Homo sapiens)Allele/Variant
Source: rs28934574
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673776G>A
(GRCh38)17:7673787G>C
(Homo sapiens)Allele/Variant
Source: rs876659802
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7673787G>C
(GRCh38)17:7674202A>C
(Homo sapiens)Allele/Variant
Source: rs1330865474
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674202A>C
(GRCh38)17:7674218T>C
(Homo sapiens)Allele/Variant
Source: rs587782082
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674218T>C
(GRCh38)17:7674225C>T
(Homo sapiens)Allele/Variant
Source: rs1019340046
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674225C>T
(GRCh38)17:7674232C>G
(Homo sapiens)Allele/Variant
Source: rs985033810
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674232C>G
(GRCh38)17:7674237G>C
(Homo sapiens)Allele/Variant
Source: rs375874539
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7674237G>C
(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)17:7675196T>G
(Homo sapiens)Allele/Variant
Source: rs2151033390
Genes: TP53 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)17:7675196T>G