Search by Gene
| geneid | 8748 |
|---|---|
| ensemblid | ENSG00000134007.5 |
| hgncid | 199 |
| symbol | ADAM20 |
| name | ADAM metallopeptidase domain 20 |
| refseq_nuc | NM_003814.5 |
| refseq_prot | NP_003805.4 |
| ensembl_nuc | ENST00000256389.5 |
| ensembl_prot | ENSP00000256389.3 |
| mane_status | MANE Select |
| chr | chr14 |
| start | 70522358 |
| end | 70535004 |
| strand | - |
| ver | v1.2 |
| region | chr14:70522358-70535004 |
| region5000 | chr14:70517358-70540004 |
| regionname0 | ADAM20_chr14_70522358_70535004 |
| regionname5000 | ADAM20_chr14_70517358_70540004 |
Multiple Alignments (by translate haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
Multiple Alignments (by aa haplotype frequency)
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aa |
|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 726 | 380 | 77 | 69 | 182 | 12 | 38 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0002 | 0/0 | 726 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0003 | 0/0 | 726 | 6 | 0 | 0 | 6 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0004 | 0/0 | 726 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0005 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0006 | 0/0 | 697 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0007 | 0/0 | 726 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2181 | 352 | 66 | 65 | 170 | 11 | 38 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0002 | 0/0 | 2181 | 26 | 9 | 4 | 12 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0003 | 0/0 | 2181 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0004 | 0/0 | 2181 | 6 | 0 | 0 | 6 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0005 | 0/0 | 2181 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0006 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0007 | 0/0 | 2181 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0008 | 0/0 | 2219 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0009 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| c0010 | 0/0 | 2181 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq |
|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 604 | 262 | 62 | 60 | 100 | 10 | 28 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| t0002 | 0/0 | 604 | 101 | 9 | 8 | 76 | 1 | 7 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| t0003 | 0/0 | 604 | 27 | 9 | 4 | 13 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| t0004 | 0/0 | 604 | 9 | 6 | 0 | 0 | 0 | 3 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| t0005 | 0/0 | 604 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| g0001 | 1/0 | 82 | 4 | 15 | 49 | 4 | 9 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0002 | 0/0 | 55 | 1 | 7 | 41 | 1 | 5 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0003 | 0/0 | 32 | 2 | 9 | 15 | 0 | 6 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0004 | 0/0 | 21 | 0 | 1 | 19 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0005 | 0/1 | 19 | 0 | 12 | 0 | 4 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0006 | 0/0 | 18 | 7 | 3 | 7 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0007 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0009 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0012 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0017 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| achapid | ahapid | chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | acseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | a0001 | c0001 | 1/1 | 352 | 66 | 65 | 170 | 11 | 38 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0002 | a0001 | c0002 | 0/0 | 26 | 9 | 4 | 12 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0006 | a0001 | c0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0010 | a0001 | c0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0002c0003 | a0002 | c0003 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0003c0004 | a0003 | c0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0004c0005 | a0004 | c0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0005c0009 | a0005 | c0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0006c0008 | a0006 | c0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0007c0007 | a0007 | c0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| acthapid | ahapid | chapid | thapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | actseq |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | a0001 | c0001 | t0001 | 1/1 | 244 | 52 | 57 | 95 | 10 | 28 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0001t0002 | a0001 | c0001 | t0002 | 0/0 | 98 | 8 | 8 | 74 | 1 | 7 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0001t0004 | a0001 | c0001 | t0004 | 0/0 | 9 | 6 | 0 | 0 | 0 | 3 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0001t0005 | a0001 | c0001 | t0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0002t0003 | a0001 | c0002 | t0003 | 0/0 | 26 | 9 | 4 | 12 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0006t0002 | a0001 | c0006 | t0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0001c0010t0001 | a0001 | c0010 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0002c0003t0001 | a0002 | c0003 | t0001 | 0/0 | 8 | 8 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0003c0004t0001 | a0003 | c0004 | t0001 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0003c0004t0002 | a0003 | c0004 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0004c0005t0001 | a0004 | c0005 | t0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0005c0009t0001 | a0005 | c0009 | t0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0006c0008t0003 | a0006 | c0008 | t0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| a0007c0007t0002 | a0007 | c0007 | t0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 | copy fasta |
| actghapid | ahapid | chapid | thapid | ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2 |
total | AFR | AMR | EAS | EUR | SAS | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | a0001 | c0001 | t0001 | g0001 | 1/0 | 82 | 4 | 15 | 49 | 4 | 9 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 32 | 2 | 9 | 15 | 0 | 6 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 0/1 | 19 | 0 | 12 | 0 | 4 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 11 | 8 | 2 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 9 | 9 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 6 | 0 | 1 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0011 | a0001 | c0001 | t0001 | g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 4 | 3 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0036 | a0001 | c0001 | t0001 | g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0062 | a0001 | c0001 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0073 | a0001 | c0001 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0088 | a0001 | c0001 | t0001 | g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0089 | a0001 | c0001 | t0001 | g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0002 | a0001 | c0001 | t0002 | g0002 | 0/0 | 55 | 1 | 7 | 41 | 1 | 5 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0004 | a0001 | c0001 | t0002 | g0004 | 0/0 | 21 | 0 | 1 | 19 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0013 | a0001 | c0001 | t0002 | g0013 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0018 | a0001 | c0001 | t0002 | g0018 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0024 | a0001 | c0001 | t0002 | g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0041 | a0001 | c0001 | t0002 | g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0042 | a0001 | c0001 | t0002 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0043 | a0001 | c0001 | t0002 | g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0044 | a0001 | c0001 | t0002 | g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0045 | a0001 | c0001 | t0002 | g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0046 | a0001 | c0001 | t0002 | g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0048 | a0001 | c0001 | t0002 | g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0049 | a0001 | c0001 | t0002 | g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0050 | a0001 | c0001 | t0002 | g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0051 | a0001 | c0001 | t0002 | g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0052 | a0001 | c0001 | t0002 | g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0053 | a0001 | c0001 | t0002 | g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0002g0056 | a0001 | c0001 | t0002 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0004g0017 | a0001 | c0001 | t0004 | g0017 | 0/0 | 3 | 1 | 0 | 0 | 0 | 2 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0004g0022 | a0001 | c0001 | t0004 | g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0004g0040 | a0001 | c0001 | t0004 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0004g0061 | a0001 | c0001 | t0004 | g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0004g0065 | a0001 | c0001 | t0004 | g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0001t0005g0076 | a0001 | c0001 | t0005 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0002t0003g0006 | a0001 | c0002 | t0003 | g0006 | 0/0 | 18 | 7 | 3 | 7 | 1 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0002t0003g0012 | a0001 | c0002 | t0003 | g0012 | 0/0 | 5 | 2 | 0 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0002t0003g0098 | a0001 | c0002 | t0003 | g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0002t0003g0100 | a0001 | c0002 | t0003 | g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0002t0003g0101 | a0001 | c0002 | t0003 | g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0006t0002g0054 | a0001 | c0006 | t0002 | g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0001c0010t0001g0077 | a0001 | c0010 | t0001 | g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0002c0003t0001g0037 | a0002 | c0003 | t0001 | g0037 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0002c0003t0001g0038 | a0002 | c0003 | t0001 | g0038 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0002c0003t0001g0039 | a0002 | c0003 | t0001 | g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0002c0003t0001g0092 | a0002 | c0003 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0002c0003t0001g0094 | a0002 | c0003 | t0001 | g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0003c0004t0001g0020 | a0003 | c0004 | t0001 | g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0003c0004t0001g0034 | a0003 | c0004 | t0001 | g0034 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0003c0004t0002g0047 | a0003 | c0004 | t0002 | g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0004c0005t0001g0021 | a0004 | c0005 | t0001 | g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0005c0009t0001g0057 | a0005 | c0009 | t0001 | g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0006c0008t0003g0099 | a0006 | c0008 | t0003 | g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| a0007c0007t0002g0055 | a0007 | c0007 | t0002 | g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ADAM20_chr14_70517358_70540004 | ADAM20 |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0003 | g0006 | EUR | GBR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00280 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | FIN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00438 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00544 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00558 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00609 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00639 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00642 | hp1 | a0004 | c0005 | t0001 | g0021 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | CHS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00733 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00733 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00735 | hp2 | a0004 | c0005 | t0001 | g0021 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG00738 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01069 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01071 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01074 | hp1 | a0001 | c0002 | t0003 | g0006 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01074 | hp2 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0023 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01099 | hp2 | a0004 | c0005 | t0001 | g0021 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01106 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01168 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01175 | hp2 | a0001 | c0001 | t0001 | g0031 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01192 | hp2 | a0001 | c0002 | t0003 | g0100 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01243 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01255 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01346 | hp2 | a0001 | c0002 | t0003 | g0006 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01496 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01517 | hp2 | a0001 | c0001 | t0001 | g0063 | EUR | IBS | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01884 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01884 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01891 | hp1 | a0001 | c0001 | t0001 | g0031 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01891 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01928 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01943 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01981 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01993 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02015 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02040 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02055 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02071 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02083 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02132 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02145 | hp2 | a0002 | c0003 | t0001 | g0039 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02165 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02258 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02258 | hp2 | a0002 | c0003 | t0001 | g0092 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02280 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02300 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02300 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02451 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02572 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02572 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02602 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02602 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02615 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02622 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02647 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02723 | hp1 | a0002 | c0003 | t0001 | g0037 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02723 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02738 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02809 | hp1 | a0001 | c0001 | t0001 | g0025 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02809 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02818 | hp1 | a0001 | c0001 | t0001 | g0026 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02818 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02886 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02895 | hp1 | a0001 | c0001 | t0004 | g0017 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02895 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02896 | hp1 | a0005 | c0009 | t0001 | g0057 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02897 | hp2 | a0001 | c0001 | t0004 | g0022 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02922 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02965 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02970 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02970 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03041 | hp1 | a0002 | c0003 | t0001 | g0039 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03098 | hp1 | a0001 | c0002 | t0003 | g0012 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03098 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03130 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03139 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | ESN | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03209 | hp2 | a0001 | c0006 | t0002 | g0054 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03225 | hp2 | a0001 | c0001 | t0002 | g0018 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03239 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03239 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03453 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0026 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03486 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03492 | hp2 | a0001 | c0001 | t0001 | g0028 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03579 | hp2 | a0002 | c0003 | t0001 | g0094 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03654 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03669 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03669 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03688 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03942 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03942 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0087 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04115 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0084 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04184 | hp2 | a0001 | c0001 | t0001 | g0003 | SAS | BEB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0032 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG04228 | hp2 | a0001 | c0001 | t0004 | g0040 | SAS | STU | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18747 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18940 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18942 | hp2 | a0003 | c0004 | t0001 | g0020 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18944 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18945 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18946 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18948 | hp1 | a0007 | c0007 | t0002 | g0055 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18952 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18953 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18956 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18957 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18959 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18963 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18965 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18965 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18966 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18967 | hp2 | a0006 | c0008 | t0003 | g0099 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18968 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18969 | hp1 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18969 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18971 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18971 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18972 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0056 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18973 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18975 | hp2 | a0003 | c0004 | t0001 | g0034 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18979 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18979 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18980 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18981 | hp1 | a0003 | c0004 | t0001 | g0020 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18981 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18984 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18985 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18985 | hp2 | a0003 | c0004 | t0001 | g0020 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18988 | hp2 | a0003 | c0004 | t0001 | g0034 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18989 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18990 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18990 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18992 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18995 | hp1 | a0003 | c0004 | t0002 | g0047 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18997 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18999 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19002 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19003 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19005 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19006 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19007 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19009 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19009 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19010 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19011 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19012 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19030 | hp1 | a0001 | c0002 | t0003 | g0006 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19030 | hp2 | a0001 | c0002 | t0003 | g0012 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19043 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19054 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19054 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19055 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19057 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19058 | hp2 | a0001 | c0001 | t0005 | g0076 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19060 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19063 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19063 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19064 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19064 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19066 | hp2 | a0001 | c0002 | t0003 | g0006 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19068 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19070 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19074 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19075 | hp2 | a0001 | c0001 | t0002 | g0045 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19076 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19080 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19082 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19083 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19084 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19086 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19086 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19087 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19240 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA19240 | hp2 | a0002 | c0003 | t0001 | g0038 | AFR | YRI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20129 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ASW | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20129 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ASW | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20905 | hp1 | a0001 | c0001 | t0002 | g0002 | SAS | GIH | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20905 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01123 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02109 | hp2 | a0001 | c0002 | t0003 | g0006 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG02559 | hp2 | a0002 | c0003 | t0001 | g0038 | AFR | ACB | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | MSL | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | USA | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | USA | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA21309 | hp1 | a0001 | c0010 | t0001 | g0077 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | LWK | ADAM20_chr14_70517358_70540004 | ADAM20 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | ADAM20_chr14_70517358_70540004 | ADAM20 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | ADAM20_chr14_70517358_70540004 | ADAM20 |
| chr:pos | ref | alt | # # of ahapid:amio-acid(protein) level
|
ahapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70522609
|
G | A | 1 | a0007 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.2149C>T | p.Arg717Cys | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2533/2784 | 2149/2181 | 717/726 | chr14 | 70522609 | ||
| chr14:70522703
|
T | TAATCCTT others(31): Show |
1 | a0006 | 1 | NA18967.hp2 | frameshift_variant | HIGH | c.2017_2054dupGATAGT others(32): Show |
p.Asn686fs | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2438/2784 | 2054/2181 | 685/726 | chr14 | 70522703 | ||
| chr14:70523134
|
C | T | 1 | a0003 | 6 | NA18942.hp2 NA18975.hp2 NA18981.hp1 others(3): Show |
missense_variant | MODERATE | c.1624G>A | p.Gly542Ser | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2008/2784 | 1624/2181 | 542/726 | chr14 | 70523134 | ||
| chr14:70523230
|
T | C | 1 | a0002 | 8 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
missense_variant | MODERATE | c.1528A>G | p.Asn510Asp | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1912/2784 | 1528/2181 | 510/726 | chr14 | 70523230 | ||
| chr14:70523238
|
G | C | 1 | a0004 | 3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
missense_variant | MODERATE | c.1520C>G | p.Thr507Arg | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1904/2784 | 1520/2181 | 507/726 | chr14 | 70523238 | ||
| chr14:70523882
|
T | G | 1 | a0005 | 1 | HG02896.hp1 | missense_variant | MODERATE | c.876A>C | p.Gln292His | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1260/2784 | 876/2181 | 292/726 | chr14 | 70523882 | ||
| chr14:70524933
|
A | C | 3 | a0001a0003a0007 | 101 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
splice_region_variant | LOW | c.-176T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | chr14 | 70524933 |
| chr:pos | ref | alt | # # of chapid
|
chapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70522676
|
C | G | 1 | a0001c0006 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.2082G>C | p.Leu694Leu | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2466/2784 | 2082/2181 | 694/726 | chr14 | 70522676 | ||
| chr14:70523045
|
T | C | 2 | a0001c0002a0006c0008 | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.1713A>G | p.Val571Val | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 2097/2784 | 1713/2181 | 571/726 | chr14 | 70523045 | ||
| chr14:70523681
|
G | A | 2 | a0001c0002a0006c0008 | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
synonymous_variant | LOW | c.1077C>T | p.Cys359Cys | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 1461/2784 | 1077/2181 | 359/726 | chr14 | 70523681 | ||
| chr14:70524284
|
T | C | 1 | a0001c0010 | 1 | NA21309.hp1 | synonymous_variant | LOW | c.474A>G | p.Val158Val | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 858/2784 | 474/2181 | 158/726 | chr14 | 70524284 |
| chr:pos | ref | alt | # # of thapid:transcript level
|
thapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70522368
|
A | C | 1 | a0001c0001t0005 | 1 | NA19058.hp2 | 3_prime_UTR_variant | MODIFIER | c.*209T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 209 | chr14 | 70522368 | |||||
| chr14:70522458
|
C | T | 1 | a0001c0001t0004 | 9 | HG02723.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*119G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 2/2 | 119 | chr14 | 70522458 | |||||
| chr14:70534947
|
G | C | 2 | a0001c0002t0003a0006c0008t0003 | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-327C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/2 | chr14 | 70534947 |
| chr:pos | ref | alt | # # of ghapid:genebody level
|
ghapids | # # of haplotypeids
|
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr14:70524971
|
G | T | 1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-176-38C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70524971 | ||||||
| chr14:70524988
|
A | G | 5 | a0002c0003t0001g0037a0002c0003t0001g0038a0002c0003t0001g0039others(2): Show | 8 | HG01884.hp1 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-176-55T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70524988 | ||||||
| chr14:70525089
|
A | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-156T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525089 | ||||||
| chr14:70525089
|
A | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-156T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525089 | ||||||
| chr14:70525150
|
C | T | 1 | a0001c0001t0001g0062 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-176-217G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525150 | ||||||
| chr14:70525216
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-283A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525216 | ||||||
| chr14:70525286
|
A | C | 1 | a0001c0001t0001g0088 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-176-353T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525286 | ||||||
| chr14:70525517
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-176-584C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525517 | ||||||
| chr14:70525540
|
A | G | 7 | a0001c0001t0001g0093a0001c0002t0003g0006a0001c0002t0003g0012others(4): Show | 28 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.-176-607T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525540 | ||||||
| chr14:70525703
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-770G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525703 | ||||||
| chr14:70525770
|
TC | T | 3 | a0001c0001t0004g0022a0001c0001t0004g0061a0001c0001t0004g0065 | 5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-838delG | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525770 | ||||||
| chr14:70525857
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-176-924C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525857 | ||||||
| chr14:70525898
|
A | C | 3 | a0001c0001t0001g0095a0001c0001t0004g0017a0001c0001t0004g0040 | 5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-965T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525898 | ||||||
| chr14:70525943
|
C | T | 3 | a0001c0001t0001g0095a0001c0001t0004g0017a0001c0001t0004g0040 | 5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-1010G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525943 | ||||||
| chr14:70525992
|
T | C | 32 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(29): Show | 132 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(129): Show |
intron_variant | MODIFIER | c.-176-1059A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70525992 | ||||||
| chr14:70526496
|
T | C | 1 | a0001c0001t0001g0067 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-176-1563A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526496 | ||||||
| chr14:70526545
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-176-1612C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526545 | ||||||
| chr14:70526602
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.-176-1669T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526602 | ||||||
| chr14:70526699
|
G | A | 1 | a0002c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-176-1766C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526699 | ||||||
| chr14:70526772
|
G | T | 4 | a0002c0003t0001g0038a0002c0003t0001g0039a0002c0003t0001g0092others(1): Show | 6 | HG02145.hp2 HG02258.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.-176-1839C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526772 | ||||||
| chr14:70526800
|
A | G | 1 | a0001c0001t0001g0014 | 4 | NA18957.hp2 NA18971.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-1867T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526800 | ||||||
| chr14:70526854
|
T | G | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1921A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526854 | ||||||
| chr14:70526855
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1922C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526855 | ||||||
| chr14:70526863
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1930G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526863 | ||||||
| chr14:70526869
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1936G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526869 | ||||||
| chr14:70526874
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1941T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526874 | ||||||
| chr14:70526875
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1942C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526875 | ||||||
| chr14:70526894
|
T | G | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1961A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526894 | ||||||
| chr14:70526906
|
A | G | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1973T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526906 | ||||||
| chr14:70526907
|
G | C | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1974C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526907 | ||||||
| chr14:70526908
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1975C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526908 | ||||||
| chr14:70526916
|
C | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1983G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526916 | ||||||
| chr14:70526917
|
T | C | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1984A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526917 | ||||||
| chr14:70526918
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1985C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526918 | ||||||
| chr14:70526922
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-1989T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526922 | ||||||
| chr14:70526933
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2000C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526933 | ||||||
| chr14:70526935
|
G | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2002C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526935 | ||||||
| chr14:70526939
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2006G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526939 | ||||||
| chr14:70526940
|
A | C | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2007T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526940 | ||||||
| chr14:70526941
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2008T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526941 | ||||||
| chr14:70526942
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2009G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526942 | ||||||
| chr14:70526942
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-176-2009G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526942 | ||||||
| chr14:70526998
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2065T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70526998 | ||||||
| chr14:70527000
|
G | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2067C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527000 | ||||||
| chr14:70527005
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2072A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527005 | ||||||
| chr14:70527019
|
C | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2086G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527019 | ||||||
| chr14:70527033
|
A | T | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2100T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527033 | ||||||
| chr14:70527040
|
T | A | 1 | a0001c0001t0002g0053 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-176-2107A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527040 | ||||||
| chr14:70527238
|
A | T | 6 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0098others(3): Show | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-2305T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527238 | ||||||
| chr14:70527323
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-176-2390C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527323 | ||||||
| chr14:70527397
|
C | G | 2 | a0001c0001t0001g0074a0001c0001t0001g0086 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-176-2464G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527397 | ||||||
| chr14:70527516
|
T | C | 3 | a0001c0001t0001g0029a0001c0001t0001g0064a0001c0001t0001g0081 | 4 | HG01243.hp1 HG02976.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-2583A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527516 | ||||||
| chr14:70527640
|
A | G | 5 | a0001c0001t0004g0017a0001c0001t0004g0022a0001c0001t0004g0040others(2): Show | 9 | HG02723.hp2 HG02818.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.-176-2707T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527640 | ||||||
| chr14:70527732
|
TG | T | 5 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(2): Show | 19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-2800delC | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527732 | ||||||
| chr14:70527763
|
C | T | 1 | a0001c0001t0001g0030 | 2 | HG02622.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.-176-2830G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527763 | ||||||
| chr14:70527861
|
T | A | 5 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(2): Show | 19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-176-2928A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527861 | ||||||
| chr14:70527894
|
C | T | 62 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 208 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(205): Show |
intron_variant | MODIFIER | c.-176-2961G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527894 | ||||||
| chr14:70527913
|
T | C | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-2980A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70527913 | ||||||
| chr14:70528043
|
T | G | 1 | a0001c0001t0002g0042 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-176-3110A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528043 | ||||||
| chr14:70528048
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0090 | 7 | HG01109.hp2 HG01175.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.-176-3115A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528048 | ||||||
| chr14:70528055
|
T | A | 1 | a0002c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-176-3122A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528055 | ||||||
| chr14:70528105
|
G | T | 53 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0010others(50): Show | 188 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.-176-3172C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528105 | ||||||
| chr14:70528116
|
A | G | 2 | a0001c0001t0002g0046a0001c0001t0002g0050 | 2 | NA18952.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.-176-3183T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528116 | ||||||
| chr14:70528198
|
A | G | 6 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0098others(3): Show | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-176-3265T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528198 | ||||||
| chr14:70528220
|
T | C | 1 | a0001c0002t0003g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-176-3287A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528220 | ||||||
| chr14:70528280
|
G | A | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3347C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528280 | ||||||
| chr14:70528281
|
A | G | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3348T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528281 | ||||||
| chr14:70528282
|
G | C | 1 | a0001c0001t0001g0027 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-176-3349C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528282 | ||||||
| chr14:70528282
|
G | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-3349C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528282 | ||||||
| chr14:70528413
|
CCTTTTCA others(4): Show |
C | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-3491_-176-348 others(15): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528413 | ||||||
| chr14:70528525
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-176-3592C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528525 | ||||||
| chr14:70528582
|
G | A | 1 | a0004c0005t0001g0021 | 3 | HG00642.hp1 HG00735.hp2 HG01099.hp2 |
intron_variant | MODIFIER | c.-176-3649C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528582 | ||||||
| chr14:70528632
|
A | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-176-3699T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528632 | ||||||
| chr14:70528677
|
A | G | 21 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0013others(18): Show | 101 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.-176-3744T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528677 | ||||||
| chr14:70528929
|
CAA | C | 3 | a0001c0001t0001g0095a0001c0001t0004g0017a0001c0001t0004g0040 | 5 | HG02145.hp1 HG02895.hp1 HG03239.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-3998_-176-399 others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528929 | ||||||
| chr14:70528985
|
T | C | 1 | a0005c0009t0001g0057 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-176-4052A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528985 | ||||||
| chr14:70528988
|
A | T | 1 | a0001c0002t0003g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.-176-4055T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70528988 | ||||||
| chr14:70529059
|
G | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(6): Show | 24 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-176-4126C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529059 | ||||||
| chr14:70529108
|
T | C | 1 | a0005c0009t0001g0057 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-176-4175A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529108 | ||||||
| chr14:70529167
|
T | C | 50 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(47): Show | 178 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.-176-4234A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529167 | ||||||
| chr14:70529194
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-176-4261G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529194 | ||||||
| chr14:70529214
|
C | A | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4281G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529214 | ||||||
| chr14:70529215
|
A | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4282T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529215 | ||||||
| chr14:70529350
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-176-4417A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529350 | ||||||
| chr14:70529388
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0096 | 7 | HG00621.hp1 HG01069.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-176-4455A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529388 | ||||||
| chr14:70529544
|
T | C | 4 | a0001c0001t0001g0029a0001c0001t0001g0064a0001c0001t0001g0080others(1): Show | 5 | HG01243.hp1 HG02976.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.-176-4611A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529544 | ||||||
| chr14:70529764
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-176-4831C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529764 | ||||||
| chr14:70529835
|
C | A | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-176-4902G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529835 | ||||||
| chr14:70529851
|
A | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(34): Show | 140 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-176-4918T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529851 | ||||||
| chr14:70529865
|
T | C | 2 | a0001c0001t0004g0022a0001c0001t0004g0065 | 4 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4932A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529865 | ||||||
| chr14:70529913
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+4884A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529913 | ||||||
| chr14:70529932
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0060 | 4 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+4865G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529932 | ||||||
| chr14:70529938
|
T | G | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4859A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529938 | ||||||
| chr14:70529939
|
G | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4858C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529939 | ||||||
| chr14:70529940
|
T | A | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4857A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70529940 | ||||||
| chr14:70530021
|
G | A | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+4776C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530021 | ||||||
| chr14:70530053
|
C | T | 1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+4744G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530053 | ||||||
| chr14:70530064
|
C | A | 1 | a0002c0003t0001g0094 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-177+4733G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530064 | ||||||
| chr14:70530132
|
T | A | 1 | a0001c0001t0001g0027 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-177+4665A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530132 | ||||||
| chr14:70530183
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-177+4614A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530183 | ||||||
| chr14:70530249
|
G | A | 1 | a0001c0001t0002g0049 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-177+4548C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530249 | ||||||
| chr14:70530436
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-177+4361T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530436 | ||||||
| chr14:70530472
|
T | G | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+4325A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530472 | ||||||
| chr14:70530579
|
G | A | 1 | a0001c0001t0002g0018 | 3 | HG02451.hp2 HG02809.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-177+4218C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530579 | ||||||
| chr14:70530591
|
G | A | 2 | a0001c0001t0002g0051a0001c0001t0002g0056 | 2 | NA18946.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.-177+4206C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530591 | ||||||
| chr14:70530690
|
A | C | 1 | a0001c0001t0001g0072 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-177+4107T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530690 | ||||||
| chr14:70530712
|
C | T | 1 | a0005c0009t0001g0057 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-177+4085G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530712 | ||||||
| chr14:70530843
|
A | C | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3954T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530843 | ||||||
| chr14:70530845
|
A | C | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3952T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530845 | ||||||
| chr14:70530846
|
G | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3951C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530846 | ||||||
| chr14:70530851
|
G | T | 1 | a0001c0001t0002g0045 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-177+3946C>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530851 | ||||||
| chr14:70530855
|
A | C | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3942T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530855 | ||||||
| chr14:70530856
|
C | G | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3941G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530856 | ||||||
| chr14:70530857
|
A | C | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3940T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530857 | ||||||
| chr14:70530859
|
A | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3938T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530859 | ||||||
| chr14:70530865
|
A | T | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+3932T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530865 | ||||||
| chr14:70530965
|
G | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(38): Show | 146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+3832C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70530965 | ||||||
| chr14:70531071
|
T | C | 6 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0098others(3): Show | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+3726A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531071 | ||||||
| chr14:70531190
|
C | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0061a0001c0001t0004g0065 | 5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+3607G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531190 | ||||||
| chr14:70531337
|
T | A | 2 | a0002c0003t0001g0038a0002c0003t0001g0039 | 4 | HG02145.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+3460A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531337 | ||||||
| chr14:70531346
|
A | G | 3 | a0001c0001t0004g0022a0001c0001t0004g0061a0001c0001t0004g0065 | 5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+3451T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531346 | ||||||
| chr14:70531413
|
G | C | 1 | a0001c0001t0001g0023 | 3 | HG01074.hp2 HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-177+3384C>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531413 | ||||||
| chr14:70531579
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-177+3218G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531579 | ||||||
| chr14:70531605
|
T | TA | 2 | a0002c0003t0001g0038a0002c0003t0001g0039 | 4 | HG02145.hp2 HG02559.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+3191dupT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531605 | ||||||
| chr14:70531629
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.-177+3168C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531629 | ||||||
| chr14:70531680
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+3117G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531680 | ||||||
| chr14:70531685
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-177+3112C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531685 | ||||||
| chr14:70531861
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(2): Show | 19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-177+2936A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531861 | ||||||
| chr14:70531946
|
T | C | 1 | a0001c0001t0001g0026 | 2 | HG02818.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.-177+2851A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70531946 | ||||||
| chr14:70532015
|
A | C | 1 | a0006c0008t0003g0099 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-177+2782T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532015 | ||||||
| chr14:70532033
|
C | T | 1 | a0001c0001t0001g0070 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-177+2764G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532033 | ||||||
| chr14:70532116
|
G | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(38): Show | 146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+2681C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532116 | ||||||
| chr14:70532203
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0053 | 2 | NA18997.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.-177+2594A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532203 | ||||||
| chr14:70532231
|
A | G | 5 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(2): Show | 19 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(16): Show |
intron_variant | MODIFIER | c.-177+2566T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532231 | ||||||
| chr14:70532257
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2540A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532257 | ||||||
| chr14:70532307
|
C | T | 6 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0098others(3): Show | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+2490G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532307 | ||||||
| chr14:70532378
|
C | A | 41 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(38): Show | 146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+2419G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532378 | ||||||
| chr14:70532378
|
C | G | 2 | a0001c0001t0001g0011a0001c0001t0001g0035 | 7 | HG02523.hp1 NA18952.hp1 NA18968.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+2419G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532378 | ||||||
| chr14:70532453
|
A | C | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2344T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532453 | ||||||
| chr14:70532521
|
A | C | 18 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0024others(15): Show | 93 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.-177+2276T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532521 | ||||||
| chr14:70532534
|
T | G | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+2263A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532534 | ||||||
| chr14:70532589
|
C | T | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+2208G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532589 | ||||||
| chr14:70532608
|
T | C | 1 | a0001c0001t0001g0083 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.-177+2189A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532608 | ||||||
| chr14:70532672
|
C | T | 3 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033 | 10 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(7): Show |
intron_variant | MODIFIER | c.-177+2125G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532672 | ||||||
| chr14:70532760
|
T | G | 37 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(34): Show | 140 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(137): Show |
intron_variant | MODIFIER | c.-177+2037A>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532760 | ||||||
| chr14:70532826
|
A | C | 1 | a0001c0001t0002g0044 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.-177+1971T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532826 | ||||||
| chr14:70532885
|
A | AAT | 3 | a0001c0001t0004g0022a0001c0001t0004g0061a0001c0001t0004g0065 | 5 | HG02723.hp2 HG02818.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.-177+1910_-177+191 others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532885 | ||||||
| chr14:70532979
|
C | T | 6 | a0001c0002t0003g0006a0001c0002t0003g0012a0001c0002t0003g0098others(3): Show | 27 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.-177+1818G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70532979 | ||||||
| chr14:70533042
|
G | A | 1 | a0001c0001t0001g0032 | 2 | HG03710.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.-177+1755C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533042 | ||||||
| chr14:70533151
|
G | A | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0058 | 5 | HG01433.hp2 HG02647.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.-177+1646C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533151 | ||||||
| chr14:70533156
|
T | C | 5 | a0001c0001t0001g0005a0001c0001t0001g0016a0001c0001t0001g0088others(2): Show | 26 | HG00099.hp2 HG00639.hp1 HG00642.hp2 others(23): Show |
intron_variant | MODIFIER | c.-177+1641A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533156 | ||||||
| chr14:70533508
|
C | A | 9 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(6): Show | 24 | HG01243.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.-177+1289G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533508 | ||||||
| chr14:70533716
|
A | G | 1 | a0001c0001t0001g0069 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.-177+1081T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533716 | ||||||
| chr14:70533756
|
T | A | 1 | a0001c0001t0001g0060 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-177+1041A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533756 | ||||||
| chr14:70533763
|
T | TA | 4 | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0004g0022others(1): Show | 12 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.-177+1033_-177+103 others(5): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533763 | ||||||
| chr14:70533764
|
T | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0032a0001c0001t0001g0033others(2): Show | 14 | HG00280.hp1 HG00738.hp1 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.-177+1033A>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533764 | ||||||
| chr14:70533765
|
A | T | 1 | a0001c0001t0001g0068 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-177+1032T>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533765 | ||||||
| chr14:70533776
|
A | AC | 2 | a0001c0001t0001g0010a0001c0001t0001g0096 | 7 | HG00621.hp1 HG01069.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-177+1020dupG | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533776 | ||||||
| chr14:70533848
|
T | C | 41 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(38): Show | 146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+949A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70533848 | ||||||
| chr14:70534061
|
C | T | 1 | a0001c0001t0001g0084 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-177+736G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534061 | ||||||
| chr14:70534062
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+735C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534062 | ||||||
| chr14:70534074
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0067 | 2 | HG01081.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-177+723G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534074 | ||||||
| chr14:70534082
|
C | CA | 12 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0015others(9): Show | 54 | HG00609.hp2 HG00621.hp2 HG00642.hp2 others(51): Show |
intron_variant | MODIFIER | c.-177+714dupT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
C | CAA | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0090others(1): Show | 6 | HG01257.hp1 HG02071.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+713_-177+714d others(4): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
CA | C | 5 | a0001c0001t0001g0029a0001c0001t0001g0062a0001c0001t0001g0063others(2): Show | 6 | HG01243.hp1 HG01517.hp2 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.-177+714delT | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
CAAA | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0026a0001c0001t0001g0058 | 6 | HG02559.hp1 HG02647.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-177+712_-177+714d others(5): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
CAAAA | C | 9 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0025others(6): Show | 29 | HG01069.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.-177+711_-177+714d others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
CAAAAA | C | 13 | a0001c0001t0001g0059a0001c0001t0002g0004a0001c0001t0002g0013others(10): Show | 38 | HG00438.hp2 HG00558.hp2 HG01258.hp2 others(35): Show |
intron_variant | MODIFIER | c.-177+710_-177+714d others(7): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534082
|
CAAAAAA | C | 9 | a0001c0001t0002g0002a0001c0001t0002g0041a0001c0001t0002g0042others(6): Show | 63 | HG00323.hp1 HG00423.hp2 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-177+709_-177+714d others(8): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534082 | ||||||
| chr14:70534093
|
A | C | 1 | a0001c0001t0001g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-177+704T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534093 | ||||||
| chr14:70534104
|
AAAAAC | A | 5 | a0001c0001t0001g0027a0001c0002t0003g0006a0001c0002t0003g0100others(2): Show | 23 | HG00099.hp1 HG00733.hp2 HG01074.hp1 others(20): Show |
intron_variant | MODIFIER | c.-177+688_-177+692d others(7): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534104 | ||||||
| chr14:70534105
|
AAAAC | A | 3 | a0001c0001t0001g0060a0001c0001t0001g0096a0001c0002t0003g0012 | 7 | HG00621.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.-177+688_-177+691d others(6): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534105 | ||||||
| chr14:70534107
|
A | C | 3 | a0001c0001t0001g0028a0001c0001t0002g0043a0002c0003t0001g0092 | 4 | HG02258.hp2 HG03490.hp2 HG03492.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+690T>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534107 | ||||||
| chr14:70534107
|
AAC | A | 2 | a0001c0001t0001g0009a0001c0001t0004g0017 | 9 | HG00738.hp1 HG01106.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.-177+688_-177+689d others(4): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534107 | ||||||
| chr14:70534109
|
C | A | 1 | a0001c0001t0001g0023 | 3 | HG01074.hp2 HG01099.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-177+688G>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534109 | ||||||
| chr14:70534117
|
C | G | 1 | a0001c0001t0002g0042 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-177+680G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534117 | ||||||
| chr14:70534125
|
C | G | 1 | a0001c0001t0004g0061 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-177+672G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534125 | ||||||
| chr14:70534191
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0059a0001c0001t0001g0060 | 4 | HG02615.hp2 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.-177+606A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534191 | ||||||
| chr14:70534300
|
C | G | 41 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(38): Show | 146 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(143): Show |
intron_variant | MODIFIER | c.-177+497G>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534300 | ||||||
| chr14:70534383
|
G | A | 47 | a0001c0001t0001g0007a0001c0001t0001g0010a0001c0001t0001g0019others(44): Show | 173 | HG00099.hp1 HG00323.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.-177+414C>T | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534383 | ||||||
| chr14:70534505
|
C | T | 30 | a0001c0001t0001g0007a0001c0001t0001g0019a0001c0001t0001g0025others(27): Show | 125 | HG00323.hp1 HG00423.hp2 HG00438.hp2 others(122): Show |
intron_variant | MODIFIER | c.-177+292G>A | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534505 | ||||||
| chr14:70534546
|
A | G | 1 | a0001c0001t0002g0041 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-177+251T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534546 | ||||||
| chr14:70534716
|
A | G | 2 | a0001c0001t0004g0017a0001c0001t0004g0040 | 4 | HG02895.hp1 HG03239.hp2 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.-177+81T>C | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534716 | ||||||
| chr14:70534753
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-177+44A>G | ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | 70534753 |