Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CDH1 (Hsa)
(GRCh38)16:68737332G>A
(Homo sapiens)Allele/Variant
Source: rs374268061
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737332G>A
(GRCh38)16:68737477C>T
(Homo sapiens)Allele/Variant
Source: rs765134569
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737477C>T
(GRCh38)16:68737546C>T
(Homo sapiens)Allele/Variant
Source: rs1362287717
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737546C>T
(GRCh38)16:68737599C>G
(Homo sapiens)Allele/Variant
Source: rs36037011
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737599C>G
(GRCh38)16:68738425G>A
(Homo sapiens)Allele/Variant
Source: rs1057521411
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738425G>A
(GRCh38)16:68835372G>A
(Homo sapiens)Allele/Variant
Source: rs35779350
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68835372G>A
(GRCh38)16:68737432G>T
(Homo sapiens)Allele/Variant
Source: rs746464544
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737432G>T
(GRCh38)16:68737470C>T
(Homo sapiens)Allele/Variant
Source: rs587782380
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737470C>T
(GRCh38)16:68801650C>T
(Homo sapiens)Allele/Variant
Source: rs751307555
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801650C>T
(GRCh38)16:68737375C>A
(Homo sapiens)Allele/Variant
Source: rs730881658
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737375C>A
(GRCh38)16:68834114G>A
(Homo sapiens)Allele/Variant
Source: rs148655354
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68834114G>A
(GRCh38)16:68833678G>T
(Homo sapiens)Allele/Variant
Source: rs1596977076
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68833678G>T
(GRCh38)16:68833695T>G
(Homo sapiens)Allele/Variant
Source: rs576484193
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68833695T>G
(GRCh38)16:68835044T>C
(Homo sapiens)Allele/Variant
Source: rs186584057
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68835044T>C
(GRCh38)16:68811857G>C
(Homo sapiens)Allele/Variant
Source: rs1960844685
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68811857G>C
(GRCh38)16:68813413A>G
(Homo sapiens)Allele/Variant
Source: rs2152133505
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68813413A>G
(GRCh38)16:68813420A>G
(Homo sapiens)Allele/Variant
Source: rs1597896016
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68813420A>G
(GRCh38)16:68813428A>G
(Homo sapiens)Allele/Variant
Source: rs1379626654
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68813428A>G
(GRCh38)16:68813536C>T
(Homo sapiens)Allele/Variant
Source: rs200905755
Genes: CDH1 (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)16:68813536C>T
(GRCh38)16:68815626C>G
(Homo sapiens)Allele/Variant
Source: rs2152134906
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68815626C>G
(GRCh38)16:68819277C>G
(Homo sapiens)Allele/Variant
Source: rs113057579
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68819277C>G
(GRCh38)16:68819400A>G
(Homo sapiens)Allele/Variant
Source: rs2152136980
Genes: CDH1 (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)16:68819400A>G
(GRCh38)16:68815771G>A
(Homo sapiens)Allele/Variant
Source: rs2152135179
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68815771G>A
(GRCh38)16:68815778C>G
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.68815778C>G
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68815778C>G
(GRCh38)16:68819426G>A
(Homo sapiens)Allele/Variant
Source: rs886041161
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68819426G>A
(GRCh38)16:68815598C>T
(Homo sapiens)Allele/Variant
Source: rs1555516122
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68815598C>T
(GRCh38)16:68819431G>A
(Homo sapiens)Allele/Variant
Source: rs1555516597
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68819431G>A
(GRCh38)16:68822022C>G
(Homo sapiens)Allele/Variant
Source: rs1567512135
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68822022C>G
(GRCh38)16:68822026G>C
(Homo sapiens)Allele/Variant
Source: rs2152138178
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68822026G>C
(GRCh38)16:68822030C>T
(Homo sapiens)Allele/Variant
Source: rs1567512154
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68822030C>T
(GRCh38)16:68738422G>A
(Homo sapiens)Allele/Variant
Source: rs773148762
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738422G>A
(GRCh38)16:68738429G>C
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.68738429G>C
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738429G>C
(GRCh38)16:68738486A>T
(Homo sapiens)Allele/Variant
Source: rs1465475126
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738486A>T
(GRCh38)16:68738492G>A
(Homo sapiens)Allele/Variant
Source: rs117555306
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738492G>A
(GRCh38)16:68833923T>A
(Homo sapiens)Allele/Variant
Source: rs867174076
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68833923T>A
(GRCh38)16:68834120C>T
(Homo sapiens)Allele/Variant
Source: rs33956791
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68834120C>T
(GRCh38)16:68835264A>G
(Homo sapiens)Allele/Variant
Source: rs1343770513
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68835264A>G
(GRCh38)16:68737366C>G
(Homo sapiens)Allele/Variant
Source: rs876660969
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737366C>G
(GRCh38)16:68737426G>T
(Homo sapiens)Allele/Variant
Source: rs1962423346
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737426G>T
(GRCh38)16:68737427G>C
(Homo sapiens)Allele/Variant
Source: rs1555509636
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737427G>C
(GRCh38)16:68737394C>A
(Homo sapiens)Allele/Variant
Source: rs730881659
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737394C>A
(GRCh38)16:68737436C>A
(Homo sapiens)Allele/Variant
Source: rs1555509640
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68737436C>A
(GRCh38)16:68738314C>T
(Homo sapiens)Allele/Variant
Source: rs865838543
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738314C>T
(GRCh38)16:68738331G>A
(Homo sapiens)Allele/Variant
Source: rs2152114382
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738331G>A
(GRCh38)16:68738341C>T
(Homo sapiens)Allele/Variant
Source: rs1555509771
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68738341C>T
(GRCh38)16:68801831A>C
(Homo sapiens)Allele/Variant
Source: rs587782023
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801831A>C
(GRCh38)16:68801796A>C
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.68801796A>C
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801796A>C
(GRCh38)16:68801693C>G
(Homo sapiens)Allele/Variant
Source: rs587783047
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801693C>G
(GRCh38)16:68801842C>A
(Homo sapiens)Allele/Variant
Source: rs876660703
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801842C>A
(GRCh38)16:68801843A>T
(Homo sapiens)Allele/Variant
Source: rs876661106
Genes: CDH1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)16:68801843A>T