Search by Gene
| geneid | 266 |
|---|---|
| ensemblid | ENSG00000099721.16 |
| hgncid | 462 |
| symbol | AMELY |
| name | amelogenin Y-linked |
| refseq_nuc | NM_001143.2 |
| refseq_prot | NP_001134.1 |
| ensembl_nuc | ENST00000651267.2 |
| ensembl_prot | ENSP00000498344.1 |
| mane_status | MANE Select |
| chr | chrY |
| start | 6865918 |
| end | 6911752 |
| strand | - |
| ver | v1.2 |
| region | chrY:6865918-6911752 |
| region5000 | chrY:6860918-6916752 |
| regionname0 | AMELY_chrY_6865918_6911752 |
| regionname5000 | AMELY_chrY_6860918_6916752 |
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 | 192 | 122 | 18 | 19 | 62 | 5 | 16 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0002 | 0/0 | 192 | 8 | 0 | 0 | 8 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0003 | 0/0 | 192 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | 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 | 579 | 122 | 18 | 19 | 62 | 5 | 16 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| c0002 | 0/0 | 579 | 8 | 0 | 0 | 8 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| c0003 | 0/0 | 579 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | 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 | 348 | 131 | 18 | 20 | 70 | 5 | 16 | AMELY_chrY_6860918_6916752 | AMELY | 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 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0005 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMELY_chrY_6860918_6916752 | AMELY |
| g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| 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 | 122 | 18 | 19 | 62 | 5 | 16 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0002c0002 | a0002 | c0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0003c0003 | a0003 | c0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | 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 | 122 | 18 | 19 | 62 | 5 | 16 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0002c0002t0001 | a0002 | c0002 | t0001 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | copy fasta |
| a0003c0003t0001 | a0003 | c0003 | t0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY | 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 | 0/0 | 15 | 0 | 0 | 15 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0002 | a0001 | c0001 | t0001 | g0002 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0003 | a0001 | c0001 | t0001 | g0003 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0004 | a0001 | c0001 | t0001 | g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0005 | a0001 | c0001 | t0001 | g0005 | 1/0 | 3 | 0 | 1 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0006 | a0001 | c0001 | t0001 | g0006 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0007 | a0001 | c0001 | t0001 | g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0008 | a0001 | c0001 | t0001 | g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0009 | a0001 | c0001 | t0001 | g0009 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0010 | a0001 | c0001 | t0001 | g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0012 | a0001 | c0001 | t0001 | g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0013 | a0001 | c0001 | t0001 | g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0014 | a0001 | c0001 | t0001 | g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0015 | a0001 | c0001 | t0001 | g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0016 | a0001 | c0001 | t0001 | g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0017 | a0001 | c0001 | t0001 | g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0019 | a0001 | c0001 | t0001 | g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0020 | a0001 | c0001 | t0001 | g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0021 | a0001 | c0001 | t0001 | g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0022 | a0001 | c0001 | t0001 | g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0023 | a0001 | c0001 | t0001 | g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0024 | a0001 | c0001 | t0001 | g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0025 | a0001 | c0001 | t0001 | g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0026 | a0001 | c0001 | t0001 | g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0027 | a0001 | c0001 | t0001 | g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0028 | a0001 | c0001 | t0001 | g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0029 | a0001 | c0001 | t0001 | g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0030 | a0001 | c0001 | t0001 | g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0031 | a0001 | c0001 | t0001 | g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0032 | a0001 | c0001 | t0001 | g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0033 | a0001 | c0001 | t0001 | g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0034 | a0001 | c0001 | t0001 | g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0035 | a0001 | c0001 | t0001 | g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0037 | a0001 | c0001 | t0001 | g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0038 | a0001 | c0001 | t0001 | g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0039 | a0001 | c0001 | t0001 | g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0040 | a0001 | c0001 | t0001 | g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0041 | a0001 | c0001 | t0001 | g0041 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0042 | a0001 | c0001 | t0001 | g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0043 | a0001 | c0001 | t0001 | g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0044 | a0001 | c0001 | t0001 | g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0045 | a0001 | c0001 | t0001 | g0045 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0046 | a0001 | c0001 | t0001 | g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0047 | a0001 | c0001 | t0001 | g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0048 | a0001 | c0001 | t0001 | g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0049 | a0001 | c0001 | t0001 | g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0050 | a0001 | c0001 | t0001 | g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0051 | a0001 | c0001 | t0001 | g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0052 | a0001 | c0001 | t0001 | g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0053 | a0001 | c0001 | t0001 | g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0054 | a0001 | c0001 | t0001 | g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0055 | a0001 | c0001 | t0001 | g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0056 | a0001 | c0001 | t0001 | g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0057 | a0001 | c0001 | t0001 | g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0058 | a0001 | c0001 | t0001 | g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0059 | a0001 | c0001 | t0001 | g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0060 | a0001 | c0001 | t0001 | g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0061 | a0001 | c0001 | t0001 | g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0063 | a0001 | c0001 | t0001 | g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0064 | a0001 | c0001 | t0001 | g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0066 | a0001 | c0001 | t0001 | g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0067 | a0001 | c0001 | t0001 | g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0068 | a0001 | c0001 | t0001 | g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0069 | a0001 | c0001 | t0001 | g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0070 | a0001 | c0001 | t0001 | g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0071 | a0001 | c0001 | t0001 | g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0072 | a0001 | c0001 | t0001 | g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0074 | a0001 | c0001 | t0001 | g0074 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0075 | a0001 | c0001 | t0001 | g0075 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0076 | a0001 | c0001 | t0001 | g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0077 | a0001 | c0001 | t0001 | g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0078 | a0001 | c0001 | t0001 | g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0079 | a0001 | c0001 | t0001 | g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0080 | a0001 | c0001 | t0001 | g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0081 | a0001 | c0001 | t0001 | g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0082 | a0001 | c0001 | t0001 | g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0083 | a0001 | c0001 | t0001 | g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0084 | a0001 | c0001 | t0001 | g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0085 | a0001 | c0001 | t0001 | g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0086 | a0001 | c0001 | t0001 | g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0087 | a0001 | c0001 | t0001 | g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0090 | a0001 | c0001 | t0001 | g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0091 | a0001 | c0001 | t0001 | g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0092 | a0001 | c0001 | t0001 | g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0093 | a0001 | c0001 | t0001 | g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0094 | a0001 | c0001 | t0001 | g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0095 | a0001 | c0001 | t0001 | g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0096 | a0001 | c0001 | t0001 | g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0001c0001t0001g0097 | a0001 | c0001 | t0001 | g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0011 | a0002 | c0002 | t0001 | g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0018 | a0002 | c0002 | t0001 | g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0062 | a0002 | c0002 | t0001 | g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0065 | a0002 | c0002 | t0001 | g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0073 | a0002 | c0002 | t0001 | g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0088 | a0002 | c0002 | t0001 | g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0002c0002t0001g0089 | a0002 | c0002 | t0001 | g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| a0003c0003t0001g0036 | a0003 | c0003 | t0001 | g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | AMELY_chrY_6860918_6916752 | AMELY |
| sampleid | haplotypeid | ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename |
|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0039 | EUR | GBR | AMELY_chrY_6860918_6916752 | AMELY |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0075 | EUR | FIN | AMELY_chrY_6860918_6916752 | AMELY |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | AMELY_chrY_6860918_6916752 | AMELY |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | AMELY_chrY_6860918_6916752 | AMELY |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | AMELY_chrY_6860918_6916752 | AMELY |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0051 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01192 | hp1 | a0003 | c0003 | t0001 | g0036 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01243 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | AMELY_chrY_6860918_6916752 | AMELY |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01256 | hp1 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0084 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0050 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | AMELY_chrY_6860918_6916752 | AMELY |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0074 | EUR | IBS | AMELY_chrY_6860918_6916752 | AMELY |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | AMELY_chrY_6860918_6916752 | AMELY |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | AMELY_chrY_6860918_6916752 | AMELY |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PEL | AMELY_chrY_6860918_6916752 | AMELY |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PEL | AMELY_chrY_6860918_6916752 | AMELY |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02055 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | AMELY_chrY_6860918_6916752 | AMELY |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | AMELY_chrY_6860918_6916752 | AMELY |
| HG02145 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | ACB | AMELY_chrY_6860918_6916752 | AMELY |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | ACB | AMELY_chrY_6860918_6916752 | AMELY |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | AMELY_chrY_6860918_6916752 | AMELY |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | GWD | AMELY_chrY_6860918_6916752 | AMELY |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG02717 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | AMELY_chrY_6860918_6916752 | AMELY |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | AMELY_chrY_6860918_6916752 | AMELY |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | AMELY_chrY_6860918_6916752 | AMELY |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0020 | AFR | MSL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | AMELY_chrY_6860918_6916752 | AMELY |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | AMELY_chrY_6860918_6916752 | AMELY |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | MSL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0055 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03654 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0037 | SAS | STU | AMELY_chrY_6860918_6916752 | AMELY |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | AMELY_chrY_6860918_6916752 | AMELY |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | AMELY_chrY_6860918_6916752 | AMELY |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | STU | AMELY_chrY_6860918_6916752 | AMELY |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | STU | AMELY_chrY_6860918_6916752 | AMELY |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | AMELY_chrY_6860918_6916752 | AMELY |
| HG04228 | hp1 | a0001 | c0001 | t0001 | g0010 | SAS | STU | AMELY_chrY_6860918_6916752 | AMELY |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | YRI | AMELY_chrY_6860918_6916752 | AMELY |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHB | AMELY_chrY_6860918_6916752 | AMELY |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | CHB | AMELY_chrY_6860918_6916752 | AMELY |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18943 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18944 | hp1 | a0002 | c0002 | t0001 | g0018 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18948 | hp1 | a0002 | c0002 | t0001 | g0062 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18967 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18971 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18983 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19000 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19012 | hp1 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19043 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | LWK | AMELY_chrY_6860918_6916752 | AMELY |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19058 | hp1 | a0002 | c0002 | t0001 | g0011 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19068 | hp1 | a0002 | c0002 | t0001 | g0065 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19082 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | AMELY_chrY_6860918_6916752 | AMELY |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0045 | EUR | TSI | AMELY_chrY_6860918_6916752 | AMELY |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | GIH | AMELY_chrY_6860918_6916752 | AMELY |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ACB | AMELY_chrY_6860918_6916752 | AMELY |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | MSL | AMELY_chrY_6860918_6916752 | AMELY |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | AMELY_chrY_6860918_6916752 | AMELY |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0041 | REF | REF | AMELY_chrY_6860918_6916752 | AMELY |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0005 | REF | REF | AMELY_chrY_6860918_6916752 | AMELY |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrY:6868113
|
C | T | 1 | a0002 | 8 | NA18944.hp1 NA18948.hp1 NA18967.hp1 others(5): Show |
missense_variant | MODERATE | c.497G>A | p.Arg166Gln | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/7 | 689/926 | 497/579 | 166/192 | chrY | 6868113 | ||
| chrY:6868402
|
C | T | 1 | a0003 | 1 | HG01192.hp1 | missense_variant | MODERATE | c.208G>A | p.Val70Met | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/7 | 400/926 | 208/579 | 70/192 | chrY | 6868402 |
| 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 |
|---|
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrY:6866227
|
G | A | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.574-149C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6866227 | ||||||
| chrY:6866639
|
C | CT | 12 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0022others(9): Show | 13 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
intron_variant | MODIFIER | c.574-562dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6866639 | ||||||
| chrY:6866639
|
CT | C | 2 | a0001c0001t0001g0025a0001c0001t0001g0053 | 2 | HG03490.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.574-562delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6866639 | ||||||
| chrY:6866835
|
T | C | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.574-757A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6866835 | ||||||
| chrY:6867320
|
C | T | 1 | a0001c0001t0001g0021 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.573+717G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6867320 | ||||||
| chrY:6867468
|
G | C | 1 | a0001c0001t0001g0094 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.573+569C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6867468 | ||||||
| chrY:6867545
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.573+492A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6867545 | ||||||
| chrY:6867563
|
G | GT | 1 | a0001c0001t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.573+473dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 6/6 | chrY | 6867563 | ||||||
| chrY:6868533
|
CTT | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0079others(1): Show | 4 | HG00673.hp1 HG02071.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.148-73_148-72delAA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 5/6 | chrY | 6868533 | ||||||
| chrY:6868558
|
T | C | 1 | a0001c0001t0001g0061 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.148-96A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 5/6 | chrY | 6868558 | ||||||
| chrY:6869219
|
G | GA | 1 | a0001c0001t0001g0027 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.103-444dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 4/6 | chrY | 6869219 | ||||||
| chrY:6869481
|
T | TA | 8 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0040others(5): Show | 9 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(6): Show |
intron_variant | MODIFIER | c.102+524dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 4/6 | chrY | 6869481 | ||||||
| chrY:6870313
|
T | TAAAGTTG others(345): Show |
1 | a0001c0001t0001g0029 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.55-261_55-260insTT others(350): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6870313 | ||||||
| chrY:6871380
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.54+1175T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871380 | ||||||
| chrY:6871785
|
C | A | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.54+770G>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871785 | ||||||
| chrY:6871816
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18971.hp1 NA18974.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.54+739G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871816 | ||||||
| chrY:6871960
|
A | AAAC | 1 | a0001c0001t0001g0040 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.54+592_54+594dupGT others(1): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871960 | ||||||
| chrY:6871960
|
AAAC | A | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.54+592_54+594delGT others(1): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871960 | ||||||
| chrY:6871993
|
C | A | 5 | a0001c0001t0001g0038a0001c0001t0001g0060a0001c0001t0001g0075others(2): Show | 5 | HG00280.hp1 HG03225.hp1 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.54+562G>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871993 | ||||||
| chrY:6871996
|
A | C | 1 | a0001c0001t0001g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.54+559T>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6871996 | ||||||
| chrY:6872305
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.54+250T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 3/6 | chrY | 6872305 | ||||||
| chrY:6872663
|
A | G | 1 | a0001c0001t0001g0042 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.-12-43T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 2/6 | chrY | 6872663 | ||||||
| chrY:6873129
|
G | C | 1 | a0001c0001t0001g0016 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-12-509C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 2/6 | chrY | 6873129 | ||||||
| chrY:6876499
|
T | C | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-112-2428A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6876499 | ||||||
| chrY:6876581
|
G | C | 3 | a0001c0001t0001g0024a0001c0001t0001g0060a0001c0001t0001g0097 | 3 | HG02647.hp1 HG03225.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.-112-2510C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6876581 | ||||||
| chrY:6876809
|
A | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-112-2738T>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6876809 | ||||||
| chrY:6876861
|
C | T | 1 | a0001c0001t0001g0009 | 2 | HG01099.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-112-2790G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6876861 | ||||||
| chrY:6877471
|
C | T | 5 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0041others(2): Show | 6 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-3400G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6877471 | ||||||
| chrY:6877964
|
T | TTG | 8 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(5): Show | 10 | HG02647.hp1 HG03490.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.-112-3895_-112-389 others(6): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6877964 | ||||||
| chrY:6879214
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-112-5143G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6879214 | ||||||
| chrY:6880722
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0047 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-112-6651A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6880722 | ||||||
| chrY:6880732
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-112-6661G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6880732 | ||||||
| chrY:6881187
|
A | C | 1 | a0001c0001t0001g0068 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-112-7116T>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6881187 | ||||||
| chrY:6881365
|
G | A | 16 | a0001c0001t0001g0003a0001c0001t0001g0019a0001c0001t0001g0023others(13): Show | 20 | NA18940.hp1 NA18944.hp1 NA18948.hp1 others(17): Show |
intron_variant | MODIFIER | c.-112-7294C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6881365 | ||||||
| chrY:6882734
|
T | G | 12 | a0001c0001t0001g0002a0001c0001t0001g0020a0001c0001t0001g0059others(9): Show | 17 | HG01074.hp1 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.-112-8663A>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6882734 | ||||||
| chrY:6882928
|
TA | T | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-8858delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6882928 | ||||||
| chrY:6883268
|
A | G | 5 | a0001c0001t0001g0008a0001c0001t0001g0022a0001c0001t0001g0041others(2): Show | 6 | HG01069.hp1 HG01255.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.-112-9197T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6883268 | ||||||
| chrY:6883368
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-112-9297G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6883368 | ||||||
| chrY:6883736
|
G | C | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-112-9665C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6883736 | ||||||
| chrY:6884018
|
G | A | 1 | a0001c0001t0001g0066 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-112-9947C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6884018 | ||||||
| chrY:6884041
|
A | G | 2 | a0001c0001t0001g0009a0001c0001t0001g0044 | 3 | HG01099.hp1 HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-112-9970T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6884041 | ||||||
| chrY:6884449
|
T | A | 1 | a0001c0001t0001g0050 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-112-10378A>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6884449 | ||||||
| chrY:6884736
|
C | G | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-112-10665G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6884736 | ||||||
| chrY:6884921
|
G | C | 1 | a0001c0001t0001g0096 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.-112-10850C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6884921 | ||||||
| chrY:6885059
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-112-10988G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885059 | ||||||
| chrY:6885212
|
A | G | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-112-11141T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885212 | ||||||
| chrY:6885217
|
T | C | 26 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(23): Show | 44 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(41): Show |
intron_variant | MODIFIER | c.-112-11146A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885217 | ||||||
| chrY:6885224
|
A | C | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-112-11153T>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885224 | ||||||
| chrY:6885246
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(2): Show | 7 | NA18612.hp1 NA18971.hp1 NA18974.hp1 others(4): Show |
intron_variant | MODIFIER | c.-112-11175T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885246 | ||||||
| chrY:6885250
|
G | C | 6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 8 | HG03225.hp1 NA18612.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-11179C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885250 | ||||||
| chrY:6885254
|
C | T | 6 | a0001c0001t0001g0006a0001c0001t0001g0012a0001c0001t0001g0013others(3): Show | 8 | HG03225.hp1 NA18612.hp1 NA18971.hp1 others(5): Show |
intron_variant | MODIFIER | c.-112-11183G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885254 | ||||||
| chrY:6885259
|
CA | C | 2 | a0001c0001t0001g0009a0001c0001t0001g0044 | 3 | HG01099.hp1 HG03579.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.-112-11189delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885259 | ||||||
| chrY:6885262
|
G | T | 56 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(53): Show | 84 | HG00140.hp1 HG00609.hp1 HG00621.hp1 others(81): Show |
intron_variant | MODIFIER | c.-112-11191C>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885262 | ||||||
| chrY:6885265
|
G | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0044a0001c0001t0001g0064others(1): Show | 5 | HG01074.hp1 HG01099.hp1 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.-112-11194C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885265 | ||||||
| chrY:6885272
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-112-11201C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885272 | ||||||
| chrY:6885275
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-112-11204G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885275 | ||||||
| chrY:6885282
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-112-11211T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885282 | ||||||
| chrY:6885407
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.-112-11336T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885407 | ||||||
| chrY:6885408
|
G | C | 1 | a0001c0001t0001g0078 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-112-11337C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885408 | ||||||
| chrY:6885418
|
G | T | 2 | a0001c0001t0001g0038a0001c0001t0001g0075 | 2 | HG00280.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.-112-11347C>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885418 | ||||||
| chrY:6885470
|
A | G | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 122 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.-112-11399T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885470 | ||||||
| chrY:6885478
|
G | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(37): Show | 52 | HG01074.hp1 HG01099.hp1 HG01106.hp1 others(49): Show |
intron_variant | MODIFIER | c.-112-11407C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885478 | ||||||
| chrY:6885601
|
T | TA | 1 | a0001c0001t0001g0090 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-112-11531dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6885601 | ||||||
| chrY:6886045
|
G | C | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-112-11974C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6886045 | ||||||
| chrY:6886064
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0047 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-112-11993C>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6886064 | ||||||
| chrY:6886143
|
TA | T | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-12073delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6886143 | ||||||
| chrY:6886322
|
GA | G | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-12252delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6886322 | ||||||
| chrY:6886449
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0090 | 2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-112-12378C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6886449 | ||||||
| chrY:6888135
|
C | T | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0079others(1): Show | 4 | HG00673.hp1 HG02071.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-112-14064G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888135 | ||||||
| chrY:6888236
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0070 | 2 | NA18966.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.-112-14165A>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888236 | ||||||
| chrY:6888326
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-112-14255T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888326 | ||||||
| chrY:6888514
|
TA | T | 1 | a0001c0001t0001g0026 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-112-14444delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888514 | ||||||
| chrY:6888867
|
C | CA | 69 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(66): Show | 99 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(96): Show |
intron_variant | MODIFIER | c.-112-14797dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888867 | ||||||
| chrY:6888867
|
C | CAA | 14 | a0001c0001t0001g0004a0001c0001t0001g0026a0001c0001t0001g0033others(11): Show | 16 | HG00673.hp1 HG01109.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.-112-14798_-112-14 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888867 | ||||||
| chrY:6888867
|
C | CAAA | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-112-14799_-112-14 others(9): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888867 | ||||||
| chrY:6888867
|
CA | C | 1 | a0001c0001t0001g0049 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-112-14797delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888867 | ||||||
| chrY:6888911
|
TA | T | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-14841delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6888911 | ||||||
| chrY:6889305
|
CT | C | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-15235delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889305 | ||||||
| chrY:6889653
|
A | G | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-112-15582T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889653 | ||||||
| chrY:6889680
|
T | G | 1 | a0001c0001t0001g0031 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-112-15609A>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889680 | ||||||
| chrY:6889793
|
T | A | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-112-15722A>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889793 | ||||||
| chrY:6889795
|
G | GT | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-15725dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889795 | ||||||
| chrY:6889984
|
CA | C | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-112-15914delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6889984 | ||||||
| chrY:6890580
|
A | T | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-112-16509T>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6890580 | ||||||
| chrY:6891000
|
A | G | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-112-16929T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6891000 | ||||||
| chrY:6891377
|
C | T | 2 | a0001c0001t0001g0037a0001c0001t0001g0047 | 2 | HG03688.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-112-17306G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6891377 | ||||||
| chrY:6893524
|
T | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0079others(1): Show | 4 | HG00673.hp1 HG02071.hp1 HG02129.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+18149A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6893524 | ||||||
| chrY:6894450
|
TC | T | 1 | a0001c0001t0001g0013 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-113+17222delG | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6894450 | ||||||
| chrY:6894830
|
CAAAT | C | 1 | a0001c0001t0001g0051 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-113+16839_-113+16 others(10): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6894830 | ||||||
| chrY:6895612
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-113+16061A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6895612 | ||||||
| chrY:6895698
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18971.hp1 NA18974.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+15975G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6895698 | ||||||
| chrY:6896014
|
A | C | 2 | a0001c0001t0001g0016a0001c0001t0001g0094 | 2 | HG02132.hp1 HG02698.hp1 |
intron_variant | MODIFIER | c.-113+15659T>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6896014 | ||||||
| chrY:6897534
|
G | A | 2 | a0001c0001t0001g0022a0001c0001t0001g0046 | 2 | HG01069.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.-113+14139C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897534 | ||||||
| chrY:6897580
|
CT | C | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-113+14092delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897580 | ||||||
| chrY:6897599
|
G | GT | 12 | a0001c0001t0001g0023a0001c0001t0001g0027a0001c0001t0001g0047others(9): Show | 12 | HG01358.hp1 HG02027.hp1 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-113+14073dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897599 | ||||||
| chrY:6897599
|
G | GTT | 1 | a0001c0001t0001g0037 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-113+14072_-113+14 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897599 | ||||||
| chrY:6897599
|
GT | G | 1 | a0001c0001t0001g0070 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-113+14073delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897599 | ||||||
| chrY:6897790
|
C | CT | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+13882dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897790 | ||||||
| chrY:6897817
|
C | T | 1 | a0003c0003t0001g0036 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-113+13856G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897817 | ||||||
| chrY:6897993
|
T | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(87): Show | 122 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.-113+13680A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6897993 | ||||||
| chrY:6898171
|
G | GC | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+13501dupG | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898171 | ||||||
| chrY:6898370
|
T | C | 1 | a0001c0001t0001g0047 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-113+13303A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898370 | ||||||
| chrY:6898383
|
CA | C | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+13289delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898383 | ||||||
| chrY:6898707
|
G | GA | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+12965_-113+12 others(7): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898707 | ||||||
| chrY:6898710
|
GA | G | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+12962delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898710 | ||||||
| chrY:6898951
|
GA | G | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+12721delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6898951 | ||||||
| chrY:6899225
|
AT | A | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+12447delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899225 | ||||||
| chrY:6899244
|
T | C | 1 | a0001c0001t0001g0048 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-113+12429A>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899244 | ||||||
| chrY:6899394
|
C | CA | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+12278_-113+12 others(7): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899394 | ||||||
| chrY:6899394
|
C | G | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | NA18940.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.-113+12279G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899394 | ||||||
| chrY:6899537
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-113+12136G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899537 | ||||||
| chrY:6899733
|
C | CA | 1 | a0001c0001t0001g0034 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.-113+11939dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899733 | ||||||
| chrY:6899918
|
AC | A | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+11754delG | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899918 | ||||||
| chrY:6899968
|
C | G | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-113+11705G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6899968 | ||||||
| chrY:6900721
|
G | GA | 2 | a0001c0001t0001g0071a0001c0001t0001g0093 | 2 | HG01928.hp1 HG02258.hp1 |
intron_variant | MODIFIER | c.-113+10951dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6900721 | ||||||
| chrY:6900838
|
C | T | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-113+10835G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6900838 | ||||||
| chrY:6900844
|
C | CT | 75 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(72): Show | 106 | HG00140.hp1 HG00280.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.-113+10828dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6900844 | ||||||
| chrY:6900844
|
C | CTT | 10 | a0001c0001t0001g0012a0001c0001t0001g0017a0001c0001t0001g0020others(7): Show | 10 | HG01074.hp1 HG01106.hp1 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.-113+10827_-113+10 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6900844 | ||||||
| chrY:6900889
|
G | A | 22 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(19): Show | 40 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(37): Show |
intron_variant | MODIFIER | c.-113+10784C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6900889 | ||||||
| chrY:6901095
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-113+10578C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6901095 | ||||||
| chrY:6901719
|
AG | A | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-113+9953delC | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6901719 | ||||||
| chrY:6901970
|
C | T | 4 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(1): Show | 4 | NA18971.hp1 NA18974.hp1 NA18989.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+9703G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6901970 | ||||||
| chrY:6902205
|
GA | G | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+9467delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6902205 | ||||||
| chrY:6902558
|
C | CT | 1 | a0001c0001t0001g0060 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-113+9114dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6902558 | ||||||
| chrY:6902558
|
CT | C | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+9114delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6902558 | ||||||
| chrY:6902717
|
A | AT | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-113+8955dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6902717 | ||||||
| chrY:6902717
|
AT | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0072a0001c0001t0001g0082 | 3 | HG02145.hp1 NA18953.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-113+8955delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6902717 | ||||||
| chrY:6903215
|
A | AC | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+8457_-113+845 others(5): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6903215 | ||||||
| chrY:6903374
|
CA | C | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+8298delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6903374 | ||||||
| chrY:6903442
|
TC | T | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+8230delG | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6903442 | ||||||
| chrY:6903531
|
C | T | 1 | a0001c0001t0001g0057 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-113+8142G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6903531 | ||||||
| chrY:6905460
|
CTCTT | C | 4 | a0001c0001t0001g0024a0001c0001t0001g0057a0001c0001t0001g0058others(1): Show | 4 | HG01243.hp1 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.-113+6209_-113+621 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6905460 | ||||||
| chrY:6905484
|
TTCTC | T | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-113+6185_-113+618 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6905484 | ||||||
| chrY:6905521
|
TTTCC | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0007others(20): Show | 41 | HG00609.hp1 HG00621.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.-113+6148_-113+615 others(8): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6905521 | ||||||
| chrY:6905606
|
CT | C | 2 | a0001c0001t0001g0023a0002c0002t0001g0073 | 2 | NA18967.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-113+6066delA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6905606 | ||||||
| chrY:6906696
|
G | GT | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-113+4976dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6906696 | ||||||
| chrY:6907304
|
T | TTC | 1 | a0001c0001t0001g0026 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-113+4368_-113+436 others(6): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907304 | ||||||
| chrY:6907305
|
C | G | 1 | a0001c0001t0001g0026 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.-113+4368G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907305 | ||||||
| chrY:6907379
|
C | CAAAAAA | 1 | a0001c0001t0001g0023 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-113+4288_-113+429 others(10): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907379 | ||||||
| chrY:6907379
|
C | CAAAAAAA | 34 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(31): Show | 45 | HG01074.hp1 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.-113+4287_-113+429 others(11): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907379 | ||||||
| chrY:6907379
|
C | CAAAAAAA others(1): Show |
1 | a0001c0001t0001g0015 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.-113+4286_-113+429 others(12): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907379 | ||||||
| chrY:6907866
|
T | A | 1 | a0001c0001t0001g0074 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.-113+3807A>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907866 | ||||||
| chrY:6907902
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-113+3771C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6907902 | ||||||
| chrY:6908118
|
A | AG | 1 | a0001c0001t0001g0025 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.-113+3554dupC | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6908118 | ||||||
| chrY:6908450
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-113+3223T>G | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6908450 | ||||||
| chrY:6908456
|
C | CA | 19 | a0001c0001t0001g0007a0001c0001t0001g0015a0001c0001t0001g0017others(16): Show | 21 | HG00621.hp1 HG01258.hp1 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-113+3216dupT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6908456 | ||||||
| chrY:6908456
|
C | CAA | 2 | a0001c0001t0001g0020a0001c0001t0001g0092 | 2 | HG02055.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-113+3215_-113+321 others(6): Show |
AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6908456 | ||||||
| chrY:6908456
|
CA | C | 3 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0023 | 3 | HG01069.hp1 HG01167.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-113+3216delT | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6908456 | ||||||
| chrY:6909302
|
C | T | 1 | a0001c0001t0001g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-113+2371G>A | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6909302 | ||||||
| chrY:6909635
|
G | GT | 1 | a0001c0001t0001g0019 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-113+2037dupA | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6909635 | ||||||
| chrY:6909921
|
A | G | 1 | a0002c0002t0001g0018 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.-113+1752T>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6909921 | ||||||
| chrY:6910002
|
G | A | 5 | a0001c0001t0001g0016a0001c0001t0001g0093a0001c0001t0001g0094others(2): Show | 5 | HG01928.hp1 HG01952.hp1 HG02132.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+1671C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6910002 | ||||||
| chrY:6910626
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-113+1047C>T | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6910626 | ||||||
| chrY:6911568
|
C | G | 1 | a0001c0001t0001g0017 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.-113+105G>C | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6911568 | ||||||
| chrY:6911611
|
A | AC | 5 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0014others(2): Show | 5 | HG02698.hp1 NA18971.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-113+61dupG | AMELY | ENSG00000099721.16 | transcript | ENST00000651267.2 | protein_coding | 1/6 | chrY | 6911611 |