Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 94122 |
|---|---|
| ensemblid | ENSG00000147041.12 |
| hgncid | 15589 |
| symbol | SYTL5 |
| name | synaptotagmin like 5 |
| refseq_nuc | NM_138780.3 |
| refseq_prot | NP_620135.1 |
| ensembl_nuc | ENST00000297875.7 |
| ensembl_prot | ENSP00000297875.2 |
| mane_status | MANE Select |
| chr | chrX |
| start | 38006553 |
| end | 38128816 |
| strand | + |
| ver | v1.2 |
| region | chrX:38006553-38128816 |
| region5000 | chrX:38001553-38133816 |
| regionname0 | SYTL5_chrX_38006553_38128816 |
| regionname5000 | SYTL5_chrX_38001553_38133816 |
| 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 | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 730 | 211 | 53 | 33 | 91 | 7 | 25 | 64 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002 | 0/0 | 730 | 25 | 10 | 9 | 1 | 0 | 5 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0003 | 0/0 | 730 | 8 | 5 | 2 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0004 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0005 | 0/0 | 730 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0006 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0007 | 0/0 | 729 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0008 | 0/0 | 608 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0009 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/1 | 2193 | 137 | 5 | 24 | 79 | 7 | 20 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0002 | 0/0 | 2193 | 51 | 26 | 9 | 11 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0003 | 0/0 | 2193 | 25 | 10 | 9 | 1 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0004 | 0/0 | 2193 | 21 | 21 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0005 | 0/0 | 2193 | 8 | 5 | 2 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0006 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0008 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0009 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0010 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0011 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0012 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| c0013 | 0/0 | 2194 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| thapid | grch38chm13v2 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 2559 | 78 | 2 | 18 | 45 | 5 | 6 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0002 | 0/0 | 2559 | 63 | 43 | 10 | 6 | 0 | 4 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0003 | 0/0 | 2559 | 44 | 1 | 3 | 27 | 2 | 11 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0004 | 0/0 | 2559 | 30 | 9 | 9 | 4 | 0 | 8 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0005 | 0/0 | 2559 | 7 | 0 | 0 | 7 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0006 | 0/0 | 2559 | 5 | 4 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0007 | 0/0 | 2559 | 3 | 3 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0008 | 0/0 | 2559 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0009 | 0/0 | 2559 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0010 | 0/0 | 2559 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0011 | 0/0 | 2559 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0012 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0013 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0014 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0015 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0016 | 0/0 | 2559 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0017 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0018 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0019 | 0/0 | 2559 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0020 | 0/0 | 2559 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0021 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0022 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| t0023 | 0/0 | 2559 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| achapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2193 | 137 | 5 | 24 | 79 | 7 | 20 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002 | 0/0 | 2193 | 51 | 26 | 9 | 11 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004 | 0/0 | 2193 | 21 | 21 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0008 | 0/0 | 2193 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0010 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003 | 0/0 | 2193 | 25 | 10 | 9 | 1 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0003c0005 | 0/0 | 2193 | 8 | 5 | 2 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0004c0006 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0005c0007 | 0/0 | 2193 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0006c0009 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0007c0011 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0008c0013 | 0/0 | 2194 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0009c0012 | 0/0 | 2193 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4751 | 75 | 2 | 18 | 42 | 5 | 6 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0002 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0003 | 0/0 | 4751 | 41 | 0 | 3 | 26 | 2 | 10 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0004 | 0/0 | 4751 | 5 | 1 | 0 | 1 | 0 | 3 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0005 | 0/0 | 4751 | 6 | 0 | 0 | 6 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0006 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0008 | 0/0 | 4751 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0012 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0013 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0014 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0015 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0016 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0001t0019 | 0/0 | 4751 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0002 | 0/0 | 4751 | 42 | 24 | 8 | 6 | 0 | 4 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0004 | 0/0 | 4751 | 4 | 1 | 1 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0009 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0011 | 0/0 | 4751 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0020 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0002t0021 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0002 | 0/0 | 4751 | 10 | 10 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0003 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0004 | 0/0 | 4751 | 4 | 4 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0006 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0010 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0017 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0022 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0004t0023 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0008t0004 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0001c0010t0005 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003t0002 | 0/0 | 4751 | 5 | 5 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003t0004 | 0/0 | 4751 | 14 | 0 | 8 | 1 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003t0006 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003t0007 | 0/0 | 4751 | 3 | 3 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0002c0003t0018 | 0/0 | 4751 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0003c0005t0002 | 0/0 | 4751 | 5 | 3 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0003c0005t0003 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0003c0005t0004 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0004c0006t0001 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0005c0007t0006 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0006c0009t0001 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0007c0011t0001 | 0/0 | 4748 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0008c0013t0009 | 0/0 | 4752 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| a0009c0012t0003 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | copy fasta | chrX | 38001553 | 38133816 |
| actghapid | 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 | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0095 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0163 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0002g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0004g0003 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0004g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0008g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0012g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0013g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0014g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0015g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0016g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0019g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0004g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0004g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0004g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0004g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0009g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0011g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0011g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0020g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0021g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0003g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0010g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0010g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0017g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0022g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0023g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0008t0004g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0010t0005g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0006g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0006g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0018g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0003g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0004g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0004g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0004c0006t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0005c0007t0006g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0006c0009t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0007c0011t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0008c0013t0009g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0009c0012t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0102 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0221 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0227 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0115 | EUR | FIN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0035 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0036 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0176 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00609 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00639 | hp2 | a0001 | c0002 | t0002 | g0042 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0201 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00733 | hp1 | a0002 | c0003 | t0004 | g0094 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00735 | hp1 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0229 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0129 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01109 | hp1 | a0001 | c0002 | t0004 | g0127 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01167 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01168 | hp2 | a0002 | c0003 | t0018 | g0208 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01169 | hp1 | a0002 | c0003 | t0004 | g0002 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01175 | hp1 | a0002 | c0003 | t0004 | g0089 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01175 | hp2 | a0001 | c0002 | t0002 | g0219 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01243 | hp1 | a0002 | c0003 | t0004 | g0087 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01255 | hp1 | a0002 | c0003 | t0004 | g0167 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01256 | hp1 | a0001 | c0002 | t0002 | g0220 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01261 | hp1 | a0003 | c0005 | t0002 | g0001 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01358 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01361 | hp1 | a0002 | c0003 | t0004 | g0164 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0213 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01496 | hp1 | a0003 | c0005 | t0002 | g0001 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0145 | EUR | IBS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01884 | hp1 | a0002 | c0003 | t0002 | g0044 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01884 | hp2 | a0001 | c0002 | t0002 | g0015 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0016 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01891 | hp2 | a0001 | c0004 | t0022 | g0030 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0216 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01952 | hp1 | a0001 | c0001 | t0008 | g0098 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01993 | hp1 | a0001 | c0001 | t0019 | g0041 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0218 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0040 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0178 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0245 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0222 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02132 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02145 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0039 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02148 | hp2 | a0001 | c0001 | t0008 | g0097 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02155 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CDX | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | CDX | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0239 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0068 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0071 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0234 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02451 | hp2 | a0001 | c0002 | t0004 | g0091 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02523 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02523 | hp2 | a0001 | c0001 | t0003 | g0191 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02572 | hp1 | a0001 | c0004 | t0006 | g0171 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0008 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02630 | hp1 | a0002 | c0003 | t0006 | g0025 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02630 | hp2 | a0001 | c0004 | t0004 | g0092 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02647 | hp1 | a0001 | c0002 | t0002 | g0058 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0223 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02698 | hp1 | a0005 | c0007 | t0006 | g0065 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02717 | hp1 | a0003 | c0005 | t0002 | g0028 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0242 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0237 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0010 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02809 | hp2 | a0002 | c0003 | t0007 | g0021 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0006 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02886 | hp2 | a0001 | c0002 | t0002 | g0047 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02895 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0069 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02922 | hp2 | a0002 | c0003 | t0007 | g0022 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02970 | hp1 | a0002 | c0003 | t0006 | g0024 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0060 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03017 | hp1 | a0002 | c0003 | t0004 | g0088 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03041 | hp1 | a0001 | c0002 | t0002 | g0029 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03098 | hp1 | a0002 | c0003 | t0002 | g0046 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03130 | hp1 | a0001 | c0001 | t0002 | g0009 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03139 | hp1 | a0001 | c0004 | t0002 | g0049 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03195 | hp1 | a0001 | c0004 | t0002 | g0004 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03195 | hp2 | a0003 | c0005 | t0004 | g0235 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0027 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03453 | hp1 | a0001 | c0002 | t0021 | g0020 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0026 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0236 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03490 | hp1 | a0002 | c0003 | t0004 | g0090 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03491 | hp1 | a0003 | c0005 | t0003 | g0238 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0003 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0007 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0070 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0230 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03540 | hp2 | a0001 | c0004 | t0017 | g0231 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0055 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0155 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03669 | hp1 | a0001 | c0002 | t0020 | g0045 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03669 | hp2 | a0001 | c0001 | t0003 | g0106 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03688 | hp1 | a0002 | c0003 | t0004 | g0093 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03704 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03704 | hp2 | a0002 | c0003 | t0004 | g0085 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0125 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0177 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0224 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0037 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0187 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0043 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0143 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04115 | hp1 | a0001 | c0001 | t0003 | g0174 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04184 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04184 | hp2 | a0002 | c0003 | t0004 | g0170 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04199 | hp1 | a0001 | c0001 | t0003 | g0225 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0144 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0005 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18522 | hp1 | a0001 | c0008 | t0004 | g0160 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | CHB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18747 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0243 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18906 | hp2 | a0001 | c0001 | t0004 | g0168 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18939 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18939 | hp2 | a0004 | c0006 | t0001 | g0137 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0052 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0200 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0217 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18950 | hp2 | a0001 | c0002 | t0011 | g0032 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0054 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18954 | hp1 | a0001 | c0001 | t0016 | g0196 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0066 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0034 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0063 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18965 | hp1 | a0001 | c0001 | t0003 | g0197 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18966 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18967 | hp1 | a0008 | c0013 | t0009 | g0116 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18971 | hp1 | a0001 | c0002 | t0009 | g0084 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18977 | hp1 | a0009 | c0012 | t0003 | g0190 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18984 | hp1 | a0007 | c0011 | t0001 | g0131 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18990 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18995 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18999 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19002 | hp1 | a0001 | c0001 | t0013 | g0205 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0154 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0053 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19005 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19006 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19007 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0057 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19030 | hp1 | a0003 | c0005 | t0004 | g0161 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19030 | hp2 | a0001 | c0002 | t0002 | g0059 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19043 | hp1 | a0001 | c0004 | t0023 | g0019 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19058 | hp1 | a0001 | c0001 | t0005 | g0048 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0194 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19072 | hp1 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19077 | hp2 | a0001 | c0002 | t0004 | g0078 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0214 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19083 | hp1 | a0001 | c0001 | t0005 | g0067 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19085 | hp1 | a0006 | c0009 | t0001 | g0096 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19086 | hp1 | a0002 | c0003 | t0004 | g0158 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19089 | hp2 | a0001 | c0010 | t0005 | g0031 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19240 | hp1 | a0003 | c0005 | t0002 | g0056 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0244 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0233 | AFR | ASW | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0061 | AFR | ASW | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0083 | EUR | TSI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20805 | hp1 | a0001 | c0001 | t0003 | g0186 | EUR | TSI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0107 | SAS | GIH | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0062 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02559 | hp1 | a0001 | c0004 | t0010 | g0017 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02559 | hp2 | a0002 | c0003 | t0007 | g0023 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03471 | hp1 | a0001 | c0004 | t0010 | g0018 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG06807 | hp1 | a0001 | c0004 | t0004 | g0232 | AFR | USA | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0004 | AFR | USA | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18955 | hp1 | a0001 | c0001 | t0015 | g0165 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA21309 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0064 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0095 | REF | REF | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0163 | REF | REF | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:38089489
|
C | T | 1 | a0009 | 1 | NA18977.hp1 | missense_variant | MODERATE | c.733C>T | p.Pro245Ser | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/17 | 1205/4751 | 733/2193 | 245/730 | chrX | 38089489 | ||
| chrX:38089579
|
A | G | 1 | a0002 | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
missense_variant | MODERATE | c.823A>G | p.Ile275Val | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/17 | 1295/4751 | 823/2193 | 275/730 | chrX | 38089579 | ||
| chrX:38089583
|
G | A | 1 | a0004 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.827G>A | p.Ser276Asn | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/17 | 1299/4751 | 827/2193 | 276/730 | chrX | 38089583 | ||
| chrX:38094367
|
C | T | 1 | a0003 | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
missense_variant | MODERATE | c.904C>T | p.Arg302Cys | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/17 | 1376/4751 | 904/2193 | 302/730 | chrX | 38094367 | ||
| chrX:38094368
|
G | A | 1 | a0005 | 1 | HG02698.hp1 | missense_variant | MODERATE | c.905G>A | p.Arg302His | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/17 | 1377/4751 | 905/2193 | 302/730 | chrX | 38094368 | ||
| chrX:38106617
|
G | A | 1 | a0006 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.1180G>A | p.Val394Ile | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/17 | 1652/4751 | 1180/2193 | 394/730 | chrX | 38106617 | ||
| chrX:38122102
|
AAAG | A | 1 | a0007 | 1 | NA18984.hp1 | conservative_inframe_deletion | MODERATE | c.1735_1737delAAG | p.Lys579del | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/17 | 2207/4751 | 1735/2193 | 579/730 | INFO_REALIGN_3_PRIME | chrX | 38122102 | |
| chrX:38122147
|
G | GT | 1 | a0008 | 1 | NA18967.hp1 | frameshift_variant | HIGH | c.1775dupT | p.Ile593fs | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/17 | 2248/4751 | 1776/2193 | 592/730 | INFO_REALIGN_3_PRIME | chrX | 38122147 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:38073633
|
A | G | 4 | a0001c0002a0002c0003a0003c0005others(1): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
synonymous_variant | LOW | c.489A>G | p.Ala163Ala | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/17 | 961/4751 | 489/2193 | 163/730 | chrX | 38073633 | ||
| chrX:38094381
|
T | C | 1 | a0001c0008 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.918T>C | p.Ser306Ser | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/17 | 1390/4751 | 918/2193 | 306/730 | chrX | 38094381 | ||
| chrX:38108615
|
T | C | 6 | a0001c0002a0001c0004a0001c0008others(3): Show | 107 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(104): Show |
synonymous_variant | LOW | c.1350T>C | p.Tyr450Tyr | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/17 | 1822/4751 | 1350/2193 | 450/730 | chrX | 38108615 | ||
| chrX:38122132
|
A | G | 1 | a0001c0010 | 1 | NA19089.hp2 | synonymous_variant | LOW | c.1758A>G | p.Gly586Gly | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/17 | 2230/4751 | 1758/2193 | 586/730 | chrX | 38122132 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:38033563
|
G | C | 1 | a0002c0003t0007 | 3 | HG02559.hp2 HG02809.hp2 HG02922.hp2 |
5_prime_UTR_variant | MODIFIER | c.-327G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/17 | 327 | chrX | 38033563 | |||||
| chrX:38033743
|
C | T | 19 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(16): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-147C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/17 | chrX | 38033743 | ||||||
| chrX:38126808
|
G | A | 1 | a0001c0001t0012 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*78G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 78 | chrX | 38126808 | |||||
| chrX:38127088
|
A | G | 1 | a0001c0004t0023 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*358A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 358 | chrX | 38127088 | |||||
| chrX:38127320
|
T | G | 1 | a0001c0001t0013 | 1 | NA19002.hp1 | 3_prime_UTR_variant | MODIFIER | c.*590T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 590 | chrX | 38127320 | |||||
| chrX:38127349
|
C | T | 1 | a0002c0003t0018 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*619C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 619 | chrX | 38127349 | |||||
| chrX:38127480
|
A | G | 21 | a0001c0001t0002a0001c0001t0004a0001c0002t0002others(18): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
3_prime_UTR_variant | MODIFIER | c.*750A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 750 | chrX | 38127480 | |||||
| chrX:38127584
|
C | T | 34 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(31): Show | 161 | HG00099.hp1 HG00544.hp2 HG00558.hp1 others(158): Show |
3_prime_UTR_variant | MODIFIER | c.*854C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 854 | chrX | 38127584 | |||||
| chrX:38127622
|
A | T | 3 | a0001c0002t0009a0001c0002t0011a0008c0013t0009 | 4 | NA18940.hp1 NA18950.hp2 NA18967.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*892A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 892 | chrX | 38127622 | |||||
| chrX:38127805
|
C | T | 1 | a0001c0001t0016 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1075C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1075 | chrX | 38127805 | |||||
| chrX:38127857
|
C | G | 1 | a0001c0001t0015 | 1 | NA18955.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1127C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1127 | chrX | 38127857 | |||||
| chrX:38128012
|
G | A | 1 | a0001c0001t0014 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1282G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1282 | chrX | 38128012 | |||||
| chrX:38128020
|
G | A | 1 | a0001c0004t0010 | 2 | HG02559.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1290G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1290 | chrX | 38128020 | |||||
| chrX:38128295
|
A | G | 2 | a0001c0004t0017a0001c0004t0022 | 2 | HG01891.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1565A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1565 | chrX | 38128295 | |||||
| chrX:38128437
|
T | G | 2 | a0001c0001t0008a0001c0001t0019 | 3 | HG01952.hp1 HG01993.hp1 HG02148.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1707T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1707 | chrX | 38128437 | |||||
| chrX:38128497
|
C | T | 1 | a0001c0002t0021 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1767C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 17/17 | 1767 | chrX | 38128497 |
| 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 cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chrX:38006669
|
G | A | 1 | a0003c0005t0002g0001 | 2 | HG01261.hp1 HG01496.hp1 |
splice_donor_variant&intron_variant | HIGH | c.-357+1G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38006669 | ||||||
| chrX:38006693
|
T | A | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-357+25T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38006693 | ||||||
| chrX:38006895
|
C | A | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-357+227C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38006895 | ||||||
| chrX:38007037
|
G | T | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-357+369G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007037 | ||||||
| chrX:38007040
|
A | G | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-357+372A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007040 | ||||||
| chrX:38007205
|
G | A | 12 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0021g0020others(9): Show | 13 | HG01261.hp1 HG01496.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-357+537G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007205 | ||||||
| chrX:38007416
|
G | A | 1 | a0003c0005t0002g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-357+748G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007416 | ||||||
| chrX:38007521
|
A | T | 25 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(22): Show | 26 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(23): Show |
intron_variant | MODIFIER | c.-357+853A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007521 | ||||||
| chrX:38007805
|
A | G | 1 | a0001c0001t0003g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-357+1137A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007805 | ||||||
| chrX:38007981
|
G | T | 3 | a0001c0004t0002g0016a0001c0004t0010g0017a0001c0004t0010g0018 | 3 | HG01891.hp1 HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.-357+1313G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38007981 | ||||||
| chrX:38008011
|
C | A | 1 | a0001c0004t0022g0030 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-357+1343C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008011 | ||||||
| chrX:38008127
|
G | A | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-357+1459G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008127 | ||||||
| chrX:38008177
|
A | G | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-357+1509A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008177 | ||||||
| chrX:38008379
|
G | T | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-357+1711G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008379 | ||||||
| chrX:38008519
|
T | C | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-357+1851T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008519 | ||||||
| chrX:38008568
|
G | T | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-357+1900G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008568 | ||||||
| chrX:38008687
|
TC | T | 61 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(58): Show | 61 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(58): Show |
intron_variant | MODIFIER | c.-357+2020delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008687 | ||||||
| chrX:38008811
|
AT | A | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-357+2146delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38008811 | |||||
| chrX:38008893
|
T | C | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-357+2225T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38008893 | ||||||
| chrX:38009061
|
C | G | 1 | a0001c0001t0004g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-357+2393C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38009061 | ||||||
| chrX:38009507
|
CT | C | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-357+2842delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38009507 | |||||
| chrX:38009717
|
A | G | 1 | a0001c0001t0003g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-357+3049A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38009717 | ||||||
| chrX:38010047
|
C | T | 1 | a0001c0001t0003g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-357+3379C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010047 | ||||||
| chrX:38010105
|
T | C | 42 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-357+3437T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010105 | ||||||
| chrX:38010426
|
G | C | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-357+3758G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010426 | ||||||
| chrX:38010475
|
C | T | 78 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(75): Show | 79 | HG00099.hp2 HG00140.hp1 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.-357+3807C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010475 | ||||||
| chrX:38010948
|
C | T | 3 | a0001c0002t0002g0027a0001c0002t0002g0029a0003c0005t0002g0028 | 3 | HG02717.hp1 HG03041.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-357+4280C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010948 | ||||||
| chrX:38010972
|
A | T | 1 | a0002c0003t0004g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-357+4304A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38010972 | ||||||
| chrX:38011358
|
G | A | 42 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-357+4690G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38011358 | ||||||
| chrX:38011527
|
G | T | 1 | a0001c0004t0002g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-357+4859G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38011527 | ||||||
| chrX:38011551
|
G | A | 2 | a0001c0004t0002g0007a0001c0004t0002g0008 | 2 | HG02622.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-357+4883G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38011551 | ||||||
| chrX:38011625
|
C | T | 5 | a0001c0001t0001g0226a0001c0001t0001g0227a0001c0001t0003g0223others(2): Show | 5 | HG00140.hp1 HG00735.hp2 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.-357+4957C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38011625 | ||||||
| chrX:38011633
|
C | CA | 222 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(219): Show | 225 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(222): Show |
intron_variant | MODIFIER | c.-357+4979dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38011633 | |||||
| chrX:38011633
|
C | CAA | 18 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(15): Show | 19 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(16): Show |
intron_variant | MODIFIER | c.-357+4978_-357+497 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38011633 | |||||
| chrX:38011633
|
CAAAAAA | C | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-357+4974_-357+497 others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38011633 | |||||
| chrX:38011881
|
A | AT | 2 | a0001c0002t0011g0032a0001c0010t0005g0031 | 2 | NA18950.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.-357+5225dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38011881 | |||||
| chrX:38011881
|
A | ATT | 40 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(37): Show | 40 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(37): Show |
intron_variant | MODIFIER | c.-357+5224_-357+522 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38011881 | |||||
| chrX:38011910
|
T | C | 5 | a0001c0004t0004g0232a0001c0004t0004g0233a0001c0004t0004g0234others(2): Show | 5 | HG02451.hp1 HG03195.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.-357+5242T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38011910 | ||||||
| chrX:38012087
|
G | A | 8 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(5): Show | 8 | HG00621.hp1 HG02083.hp1 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.-357+5419G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38012087 | ||||||
| chrX:38012146
|
G | T | 1 | a0001c0002t0002g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-357+5478G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38012146 | ||||||
| chrX:38013112
|
T | A | 4 | a0001c0002t0021g0020a0002c0003t0007g0021a0002c0003t0007g0022others(1): Show | 4 | HG02559.hp2 HG02809.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.-357+6444T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013112 | ||||||
| chrX:38013213
|
C | G | 4 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0004t0002g0068others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+6545C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013213 | ||||||
| chrX:38013259
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0003g0082 | 2 | NA19005.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.-357+6591G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013259 | ||||||
| chrX:38013472
|
G | T | 1 | a0001c0001t0001g0162 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.-357+6804G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013472 | ||||||
| chrX:38013590
|
C | A | 1 | a0001c0004t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-357+6922C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013590 | ||||||
| chrX:38013790
|
G | A | 17 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(14): Show | 18 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-357+7122G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38013790 | ||||||
| chrX:38014058
|
C | A | 1 | a0001c0002t0021g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-357+7390C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38014058 | ||||||
| chrX:38014317
|
A | C | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-357+7649A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38014317 | ||||||
| chrX:38014826
|
T | C | 1 | a0001c0001t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-357+8158T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38014826 | ||||||
| chrX:38014843
|
G | A | 2 | a0001c0002t0002g0237a0001c0004t0002g0236 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-357+8175G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38014843 | ||||||
| chrX:38015043
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.-357+8375T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015043 | ||||||
| chrX:38015061
|
T | A | 17 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(14): Show | 18 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-357+8393T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015061 | ||||||
| chrX:38015220
|
T | C | 1 | a0001c0004t0002g0026 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-357+8552T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015220 | ||||||
| chrX:38015590
|
G | A | 41 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(38): Show | 41 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-357+8922G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015590 | ||||||
| chrX:38015672
|
G | A | 162 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(159): Show | 165 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.-357+9004G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015672 | ||||||
| chrX:38015705
|
TG | T | 2 | a0001c0001t0003g0159a0001c0008t0004g0160 | 2 | HG00735.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-357+9038delG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015705 | ||||||
| chrX:38015706
|
G | GT | 2 | a0001c0001t0003g0222a0001c0001t0005g0067 | 2 | HG02071.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-357+9051dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38015706 | |||||
| chrX:38015736
|
G | T | 1 | a0002c0003t0004g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.-357+9068G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015736 | ||||||
| chrX:38015774
|
G | A | 1 | a0001c0001t0003g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-357+9106G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015774 | ||||||
| chrX:38015907
|
A | G | 16 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(13): Show | 17 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(14): Show |
intron_variant | MODIFIER | c.-357+9239A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015907 | ||||||
| chrX:38016036
|
A | T | 1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-357+9368A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016036 | ||||||
| chrX:38016179
|
C | T | 1 | a0001c0002t0002g0015 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-357+9511C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016179 | ||||||
| chrX:38016241
|
T | C | 1 | a0001c0001t0006g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-357+9573T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016241 | ||||||
| chrX:38016257
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0166 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.-357+9589C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016257 | ||||||
| chrX:38016327
|
TG | T | 1 | a0001c0001t0005g0034 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-357+9664delG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38016327 | |||||
| chrX:38016425
|
T | C | 4 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(1): Show | 4 | HG00544.hp2 HG00558.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+9757T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016425 | ||||||
| chrX:38016511
|
G | A | 6 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-357+9843G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016511 | ||||||
| chrX:38016860
|
C | T | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-357+10192C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016860 | ||||||
| chrX:38016950
|
T | C | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-357+10282T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38016950 | ||||||
| chrX:38017052
|
A | G | 84 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.-357+10384A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38017052 | ||||||
| chrX:38017131
|
A | G | 10 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(7): Show | 11 | HG02055.hp1 HG02258.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.-357+10463A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38017131 | ||||||
| chrX:38017506
|
C | CTT | 17 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(14): Show | 18 | HG02055.hp1 HG02258.hp1 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.-357+10839_-357+10 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38017506 | |||||
| chrX:38017600
|
C | T | 41 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(38): Show | 41 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.-357+10932C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38017600 | ||||||
| chrX:38017824
|
A | C | 1 | a0001c0001t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-357+11156A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38017824 | ||||||
| chrX:38018018
|
G | A | 4 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0004t0002g0068others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+11350G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018018 | ||||||
| chrX:38018264
|
C | T | 42 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(39): Show | 42 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.-357+11596C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018264 | ||||||
| chrX:38018444
|
G | C | 84 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(83): Show |
intron_variant | MODIFIER | c.-357+11776G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018444 | ||||||
| chrX:38018530
|
C | T | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-357+11862C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018530 | ||||||
| chrX:38018671
|
A | G | 4 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0004t0002g0068others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+12003A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018671 | ||||||
| chrX:38018724
|
C | G | 1 | a0001c0001t0001g0221 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-357+12056C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018724 | ||||||
| chrX:38018810
|
G | T | 3 | a0001c0002t0002g0244a0001c0004t0002g0004a0002c0003t0002g0243 | 4 | HG03195.hp1 HG06807.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+12142G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38018810 | ||||||
| chrX:38019015
|
C | T | 90 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(87): Show | 92 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-357+12347C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019015 | ||||||
| chrX:38019056
|
G | T | 1 | a0001c0001t0003g0214 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-357+12388G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019056 | ||||||
| chrX:38019371
|
C | A | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-357+12703C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019371 | ||||||
| chrX:38019671
|
C | T | 9 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(6): Show | 10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-357+13003C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019671 | ||||||
| chrX:38019691
|
G | A | 4 | a0001c0001t0002g0009a0001c0004t0002g0016a0001c0004t0010g0017others(1): Show | 4 | HG01891.hp1 HG02559.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.-357+13023G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019691 | ||||||
| chrX:38019915
|
C | CTGAG | 2 | a0001c0001t0001g0095a0001c0001t0001g0169 | 2 | HG02486.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-357+13248_-357+13 others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38019915 | |||||
| chrX:38019965
|
G | A | 90 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(87): Show | 92 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-357+13297G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019965 | ||||||
| chrX:38019983
|
T | C | 4 | a0001c0001t0019g0041a0001c0002t0002g0039a0001c0002t0002g0040others(1): Show | 4 | HG00639.hp2 HG01993.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.-357+13315T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38019983 | ||||||
| chrX:38020040
|
G | A | 1 | a0001c0002t0002g0010 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-357+13372G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020040 | ||||||
| chrX:38020137
|
T | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-356-13397T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020137 | ||||||
| chrX:38020408
|
C | CAT | 8 | a0001c0001t0003g0223a0001c0001t0003g0246a0001c0002t0002g0069others(5): Show | 8 | HG01884.hp1 HG02683.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.-356-13085_-356-13 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
C | CATAT | 2 | a0001c0002t0002g0035a0002c0003t0007g0021 | 2 | HG00544.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.-356-13087_-356-13 others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CAT | C | 30 | a0001c0001t0001g0099a0001c0001t0003g0159a0001c0001t0003g0175others(27): Show | 31 | HG00597.hp1 HG00735.hp1 HG01167.hp1 others(28): Show |
intron_variant | MODIFIER | c.-356-13085_-356-13 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATAT | C | 42 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0100others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00621.hp1 others(39): Show |
intron_variant | MODIFIER | c.-356-13087_-356-13 others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATAT | C | 43 | a0001c0001t0001g0083a0001c0001t0001g0105a0001c0001t0001g0108others(40): Show | 43 | HG00558.hp2 HG00597.hp2 HG00609.hp1 others(40): Show |
intron_variant | MODIFIER | c.-356-13089_-356-13 others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(1): Show |
C | 60 | a0001c0001t0001g0072a0001c0001t0001g0075a0001c0001t0001g0076others(57): Show | 60 | HG00280.hp1 HG00544.hp1 HG00639.hp1 others(57): Show |
intron_variant | MODIFIER | c.-356-13091_-356-13 others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(3): Show |
C | 24 | a0001c0001t0001g0145a0001c0001t0001g0146a0001c0001t0001g0147others(21): Show | 26 | HG01168.hp1 HG01169.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.-356-13093_-356-13 others(16): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(5): Show |
C | 2 | a0001c0001t0001g0152a0001c0004t0010g0018 | 2 | HG03471.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.-356-13095_-356-13 others(18): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(9): Show |
C | 4 | a0001c0004t0002g0026a0001c0004t0002g0242a0002c0003t0006g0024others(1): Show | 4 | HG02630.hp1 HG02723.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-356-13099_-356-13 others(22): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(15): Show |
C | 4 | a0001c0001t0003g0153a0001c0001t0003g0155a0001c0001t0012g0154others(1): Show | 4 | HG03654.hp1 NA18955.hp1 NA18970.hp1 others(1): Show |
intron_variant | MODIFIER | c.-356-13105_-356-13 others(28): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020408
|
CATATATA others(21): Show |
C | 1 | a0001c0001t0004g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-356-13111_-356-13 others(34): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020408 | |||||
| chrX:38020440
|
TA | T | 1 | a0001c0002t0021g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.-356-13093delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020440 | ||||||
| chrX:38020441
|
ATATATAT others(2): Show |
A | 1 | a0001c0004t0002g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-356-13091_-356-13 others(15): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020441 | |||||
| chrX:38020443
|
ATATATAT | A | 2 | a0001c0001t0003g0188a0001c0004t0017g0231 | 2 | HG03540.hp2 NA18946.hp2 |
intron_variant | MODIFIER | c.-356-13089_-356-13 others(13): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020443 | |||||
| chrX:38020445
|
ATATATT | A | 1 | a0001c0001t0014g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-356-13087_-356-13 others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38020445 | |||||
| chrX:38020450
|
T | TA | 1 | a0001c0002t0002g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-356-13084_-356-13 others(7): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020450 | ||||||
| chrX:38020739
|
A | G | 100 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(97): Show | 103 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(100): Show |
intron_variant | MODIFIER | c.-356-12795A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020739 | ||||||
| chrX:38020929
|
A | G | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-356-12605A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38020929 | ||||||
| chrX:38021161
|
G | A | 10 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(7): Show | 10 | HG00544.hp2 HG00558.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.-356-12373G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38021161 | ||||||
| chrX:38021201
|
A | T | 1 | a0001c0001t0003g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-356-12333A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38021201 | ||||||
| chrX:38021286
|
G | C | 90 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(87): Show | 92 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(89): Show |
intron_variant | MODIFIER | c.-356-12248G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38021286 | ||||||
| chrX:38021814
|
C | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015 | 3 | HG01884.hp2 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-356-11720C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38021814 | ||||||
| chrX:38021942
|
C | T | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-356-11592C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38021942 | ||||||
| chrX:38022022
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-356-11512C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38022022 | ||||||
| chrX:38022465
|
C | T | 4 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0004t0002g0068others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.-356-11069C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38022465 | ||||||
| chrX:38022490
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-356-11044T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38022490 | ||||||
| chrX:38022512
|
G | C | 2 | a0001c0001t0003g0189a0009c0012t0003g0190 | 2 | NA18977.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.-356-11022G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38022512 | ||||||
| chrX:38022864
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-356-10670G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38022864 | ||||||
| chrX:38023176
|
T | C | 1 | a0001c0002t0002g0047 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.-356-10358T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023176 | ||||||
| chrX:38023493
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.-356-10041C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023493 | ||||||
| chrX:38023602
|
C | T | 1 | a0001c0001t0013g0205 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-356-9932C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023602 | ||||||
| chrX:38023757
|
C | G | 9 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(6): Show | 10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-356-9777C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023757 | ||||||
| chrX:38023912
|
T | C | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-356-9622T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023912 | ||||||
| chrX:38023914
|
AAAGT | A | 20 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0202others(17): Show | 20 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(17): Show |
intron_variant | MODIFIER | c.-356-9617_-356-961 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38023914 | |||||
| chrX:38023947
|
A | G | 107 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(104): Show | 110 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(107): Show |
intron_variant | MODIFIER | c.-356-9587A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023947 | ||||||
| chrX:38024050
|
G | GA | 53 | a0001c0001t0001g0073a0001c0001t0001g0172a0001c0001t0001g0173others(50): Show | 53 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.-356-9475dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38024050 | |||||
| chrX:38024067
|
C | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.-356-9467C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024067 | ||||||
| chrX:38024227
|
C | T | 2 | a0001c0001t0003g0200a0001c0001t0003g0246 | 2 | NA18943.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.-356-9307C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024227 | ||||||
| chrX:38024269
|
C | G | 83 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(82): Show |
intron_variant | MODIFIER | c.-356-9265C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024269 | ||||||
| chrX:38024337
|
G | A | 17 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(14): Show | 18 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-356-9197G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024337 | ||||||
| chrX:38024340
|
C | A | 9 | a0001c0002t0002g0237a0001c0002t0002g0239a0001c0002t0002g0240others(6): Show | 10 | HG02258.hp1 HG02622.hp1 HG02723.hp1 others(7): Show |
intron_variant | MODIFIER | c.-356-9194C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024340 | ||||||
| chrX:38024420
|
CT | C | 6 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-356-9105delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38024420 | |||||
| chrX:38024513
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-356-9021T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024513 | ||||||
| chrX:38024864
|
T | G | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-356-8670T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024864 | ||||||
| chrX:38024914
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-356-8620A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38024914 | ||||||
| chrX:38025112
|
T | C | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-356-8422T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38025112 | ||||||
| chrX:38025323
|
T | G | 1 | a0003c0005t0002g0001 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.-356-8211T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38025323 | ||||||
| chrX:38025534
|
G | C | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-8000G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38025534 | ||||||
| chrX:38025727
|
A | G | 13 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0237others(10): Show | 14 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.-356-7807A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38025727 | ||||||
| chrX:38025817
|
G | A | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-7717G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38025817 | ||||||
| chrX:38026101
|
G | C | 1 | a0001c0001t0003g0144 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.-356-7433G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026101 | ||||||
| chrX:38026326
|
T | C | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-356-7208T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026326 | ||||||
| chrX:38026425
|
G | A | 6 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-356-7109G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026425 | ||||||
| chrX:38026485
|
ATAGAG | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-7046_-356-704 others(9): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38026485 | |||||
| chrX:38026551
|
C | T | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-356-6983C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026551 | ||||||
| chrX:38026652
|
A | T | 1 | a0001c0004t0002g0242 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-356-6882A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026652 | ||||||
| chrX:38026680
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-356-6854C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026680 | ||||||
| chrX:38026813
|
G | A | 2 | a0001c0002t0002g0051a0001c0002t0002g0245 | 2 | HG02055.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.-356-6721G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026813 | ||||||
| chrX:38026818
|
C | T | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.-356-6716C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38026818 | ||||||
| chrX:38027074
|
T | A | 1 | a0001c0001t0003g0209 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-356-6460T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027074 | ||||||
| chrX:38027226
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-356-6308G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027226 | ||||||
| chrX:38027323
|
G | T | 1 | a0001c0001t0005g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-356-6211G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027323 | ||||||
| chrX:38027582
|
T | C | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-5952T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027582 | ||||||
| chrX:38027649
|
A | G | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-356-5885A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027649 | ||||||
| chrX:38027758
|
CT | C | 1 | a0001c0001t0005g0034 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.-356-5768delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38027758 | |||||
| chrX:38027824
|
C | CT | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.-356-5694dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38027824 | |||||
| chrX:38027824
|
CT | C | 76 | a0001c0001t0001g0105a0001c0001t0001g0113a0001c0001t0001g0114others(73): Show | 78 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.-356-5694delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38027824 | |||||
| chrX:38027824
|
CTT | C | 9 | a0001c0002t0002g0215a0001c0004t0003g0230a0001c0004t0004g0232others(6): Show | 9 | HG01358.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-356-5695_-356-569 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38027824 | |||||
| chrX:38027943
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-356-5591C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38027943 | ||||||
| chrX:38028059
|
T | C | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-5475T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028059 | ||||||
| chrX:38028176
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-356-5358G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028176 | ||||||
| chrX:38028248
|
G | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-5286G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028248 | ||||||
| chrX:38028260
|
G | A | 1 | a0001c0002t0002g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-356-5274G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028260 | ||||||
| chrX:38028268
|
T | C | 18 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(15): Show | 19 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.-356-5266T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028268 | ||||||
| chrX:38028339
|
T | C | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-5195T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028339 | ||||||
| chrX:38028346
|
C | T | 1 | a0001c0002t0002g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-356-5188C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028346 | ||||||
| chrX:38028736
|
A | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-356-4798A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028736 | ||||||
| chrX:38028806
|
A | G | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-356-4728A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028806 | ||||||
| chrX:38029102
|
G | T | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-356-4432G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38029102 | ||||||
| chrX:38029355
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-4179C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38029355 | ||||||
| chrX:38029546
|
G | C | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-3988G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38029546 | ||||||
| chrX:38029757
|
C | CAT | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-3777_-356-377 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38029757 | ||||||
| chrX:38029847
|
ATC | A | 111 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(108): Show | 114 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.-356-3684_-356-368 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38029847 | |||||
| chrX:38030153
|
C | T | 6 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-356-3381C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030153 | ||||||
| chrX:38030382
|
G | A | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-3152G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030382 | ||||||
| chrX:38030449
|
G | T | 4 | a0001c0001t0001g0112a0001c0001t0001g0140a0001c0001t0001g0141others(1): Show | 4 | HG00597.hp2 HG00673.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.-356-3085G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030449 | ||||||
| chrX:38030479
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-356-3055G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030479 | ||||||
| chrX:38030568
|
T | C | 111 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(108): Show | 114 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.-356-2966T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030568 | ||||||
| chrX:38030658
|
A | G | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-2876A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030658 | ||||||
| chrX:38031135
|
A | G | 245 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(242): Show | 249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.-356-2399A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031135 | ||||||
| chrX:38031259
|
C | T | 1 | a0001c0002t0002g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-356-2275C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031259 | ||||||
| chrX:38031303
|
C | A | 2 | a0001c0002t0002g0237a0001c0004t0002g0236 | 2 | HG02723.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-356-2231C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031303 | ||||||
| chrX:38031346
|
T | G | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-356-2188T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031346 | ||||||
| chrX:38031376
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-2158C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031376 | ||||||
| chrX:38031377
|
G | A | 2 | a0001c0001t0001g0115a0001c0001t0001g0172 | 2 | HG00280.hp1 HG01106.hp1 |
intron_variant | MODIFIER | c.-356-2157G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031377 | ||||||
| chrX:38031420
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-2114C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031420 | ||||||
| chrX:38031566
|
T | C | 10 | a0001c0002t0021g0020a0001c0004t0002g0026a0001c0004t0006g0171others(7): Show | 11 | HG01261.hp1 HG01496.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-356-1968T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38031566 | ||||||
| chrX:38032017
|
T | G | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-356-1517T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032017 | ||||||
| chrX:38032107
|
G | C | 1 | a0001c0001t0001g0105 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.-356-1427G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032107 | ||||||
| chrX:38032109
|
C | T | 2 | a0001c0001t0001g0095a0001c0001t0001g0169 | 2 | HG02486.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-356-1425C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032109 | ||||||
| chrX:38032363
|
A | T | 52 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(49): Show | 52 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.-356-1171A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032363 | ||||||
| chrX:38032458
|
A | G | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-1076A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032458 | ||||||
| chrX:38032519
|
A | G | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-1015A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032519 | ||||||
| chrX:38032537
|
GCCGCTGT others(5): Show |
G | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | NA18939.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.-356-995_-356-984d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38032537 | |||||
| chrX:38032540
|
G | T | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.-356-994G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032540 | ||||||
| chrX:38032637
|
A | G | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-897A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032637 | ||||||
| chrX:38032724
|
C | T | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.-356-810C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032724 | ||||||
| chrX:38032725
|
G | A | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-356-809G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032725 | ||||||
| chrX:38032802
|
T | A | 6 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp1 others(3): Show |
intron_variant | MODIFIER | c.-356-732T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032802 | ||||||
| chrX:38033095
|
G | A | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-439G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38033095 | ||||||
| chrX:38033143
|
A | AAAGG | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-356-383_-356-380d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | INFO_REALIGN_3_PRIME | chrX | 38033143 | |||||
| chrX:38033186
|
T | C | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.-356-348T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38033186 | ||||||
| chrX:38033376
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.-356-158C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38033376 | ||||||
| chrX:38033526
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
splice_region_variant&intron_variant | LOW | c.-356-8C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38033526 | ||||||
| chrX:38034390
|
C | T | 23 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(20): Show | 24 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.119+382C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38034390 | ||||||
| chrX:38034817
|
C | T | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.119+809C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38034817 | ||||||
| chrX:38035465
|
C | T | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+1457C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38035465 | ||||||
| chrX:38035586
|
G | A | 8 | a0001c0002t0021g0020a0001c0004t0002g0026a0002c0003t0006g0024others(5): Show | 9 | HG01261.hp1 HG01496.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.119+1578G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38035586 | ||||||
| chrX:38035590
|
C | CA | 9 | a0001c0001t0001g0086a0001c0001t0001g0149a0001c0001t0001g0213others(6): Show | 9 | HG00642.hp1 HG01192.hp1 HG01433.hp1 others(6): Show |
intron_variant | MODIFIER | c.119+1598dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38035590 | |||||
| chrX:38035590
|
CA | C | 1 | a0001c0001t0003g0199 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.119+1598delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38035590 | |||||
| chrX:38035801
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.119+1793A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38035801 | ||||||
| chrX:38036043
|
C | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+2035C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036043 | ||||||
| chrX:38036119
|
A | G | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+2111A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036119 | ||||||
| chrX:38036165
|
T | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+2157T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036165 | ||||||
| chrX:38036238
|
G | A | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.119+2230G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036238 | ||||||
| chrX:38036418
|
T | A | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+2410T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036418 | ||||||
| chrX:38036750
|
C | T | 1 | a0001c0002t0002g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.119+2742C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036750 | ||||||
| chrX:38036839
|
A | C | 111 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(108): Show | 114 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.119+2831A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38036839 | ||||||
| chrX:38037067
|
G | A | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.119+3059G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037067 | ||||||
| chrX:38037092
|
G | C | 1 | a0001c0004t0004g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.119+3084G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037092 | ||||||
| chrX:38037094
|
G | GTTTCCCA others(5): Show |
1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.119+3089_119+3100d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037094 | |||||
| chrX:38037157
|
A | G | 5 | a0001c0001t0019g0041a0001c0002t0002g0039a0001c0002t0002g0040others(2): Show | 5 | HG00639.hp2 HG01993.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+3149A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037157 | ||||||
| chrX:38037277
|
A | C | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+3269A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037277 | ||||||
| chrX:38037517
|
T | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+3509T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037517 | ||||||
| chrX:38037667
|
C | T | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+3659C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037667 | ||||||
| chrX:38037787
|
C | CCGAT | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.119+3779_119+3780i others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037787 | ||||||
| chrX:38037788
|
T | A | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.119+3780T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037788 | ||||||
| chrX:38037788
|
T | TGATA | 62 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0080others(59): Show | 64 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(61): Show |
intron_variant | MODIFIER | c.119+3825_119+3828d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
T | TGATAGAT others(1): Show |
23 | a0001c0001t0001g0083a0001c0001t0001g0099a0001c0001t0001g0138others(20): Show | 23 | HG00639.hp2 HG00733.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.119+3821_119+3828d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
T | TGATAGAT others(5): Show |
5 | a0001c0001t0001g0104a0001c0002t0002g0245a0001c0002t0004g0091others(2): Show | 5 | HG02055.hp1 HG02451.hp2 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.119+3817_119+3828d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
T | TGATAGAT others(9): Show |
2 | a0001c0001t0001g0139a0001c0002t0002g0069 | 2 | HG00544.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.119+3813_119+3828d others(18): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
TGATA | T | 33 | a0001c0001t0001g0152a0001c0001t0001g0172a0001c0001t0001g0173others(30): Show | 33 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.119+3825_119+3828d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
TGATAGAT others(1): Show |
T | 23 | a0001c0001t0001g0179a0001c0001t0001g0185a0001c0001t0001g0206others(20): Show | 23 | HG00609.hp1 HG02015.hp1 HG02080.hp2 others(20): Show |
intron_variant | MODIFIER | c.119+3821_119+3828d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037788
|
TGATAGAT others(5): Show |
T | 2 | a0001c0001t0001g0156a0001c0001t0001g0166 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.119+3817_119+3828d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037788 | |||||
| chrX:38037825
|
G | A | 19 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0202others(16): Show | 19 | HG00099.hp2 HG00642.hp1 HG00733.hp2 others(16): Show |
intron_variant | MODIFIER | c.119+3817G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037825 | ||||||
| chrX:38037825
|
G | GATAA | 1 | a0001c0001t0004g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.119+3820_119+3821i others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38037825 | |||||
| chrX:38037943
|
C | T | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+3935C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38037943 | ||||||
| chrX:38038201
|
T | TG | 1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.119+4196dupG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38038201 | |||||
| chrX:38038251
|
G | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+4243G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038251 | ||||||
| chrX:38038274
|
GC | G | 1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.119+4271delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38038274 | |||||
| chrX:38038329
|
G | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+4321G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038329 | ||||||
| chrX:38038331
|
T | A | 19 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(16): Show | 20 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.119+4323T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038331 | ||||||
| chrX:38038367
|
C | G | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+4359C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038367 | ||||||
| chrX:38038503
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.119+4495C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038503 | ||||||
| chrX:38038857
|
G | GT | 1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.119+4852dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38038857 | |||||
| chrX:38038912
|
C | G | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.119+4904C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038912 | ||||||
| chrX:38039040
|
G | T | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+5032G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039040 | ||||||
| chrX:38039287
|
A | G | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+5279A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039287 | ||||||
| chrX:38039592
|
T | C | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.119+5584T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039592 | ||||||
| chrX:38039857
|
CA | C | 3 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231 | 3 | HG02451.hp1 HG03540.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.119+5857delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38039857 | |||||
| chrX:38039865
|
A | T | 89 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(86): Show | 91 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(88): Show |
intron_variant | MODIFIER | c.119+5857A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039865 | ||||||
| chrX:38039913
|
C | A | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+5905C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039913 | ||||||
| chrX:38039947
|
G | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.119+5939G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039947 | ||||||
| chrX:38039962
|
T | A | 1 | a0001c0001t0003g0223 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.119+5954T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039962 | ||||||
| chrX:38039976
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.119+5968C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38039976 | ||||||
| chrX:38040103
|
G | A | 1 | a0001c0001t0005g0048 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.119+6095G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040103 | ||||||
| chrX:38040153
|
G | A | 1 | a0001c0002t0002g0245 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.119+6145G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040153 | ||||||
| chrX:38040173
|
C | CA | 1 | a0001c0001t0001g0117 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.119+6179dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38040173 | |||||
| chrX:38040173
|
CA | C | 92 | a0001c0001t0001g0136a0001c0001t0002g0009a0001c0001t0005g0034others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.119+6179delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38040173 | |||||
| chrX:38040330
|
A | C | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+6322A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040330 | ||||||
| chrX:38040414
|
G | A | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.119+6406G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040414 | ||||||
| chrX:38040454
|
T | TC | 3 | a0001c0001t0001g0149a0001c0001t0003g0189a0001c0002t0002g0043 | 3 | HG02738.hp1 HG03927.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.119+6455dupC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38040454 | |||||
| chrX:38040454
|
TC | T | 1 | a0001c0002t0002g0029 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.119+6455delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38040454 | |||||
| chrX:38040455
|
C | G | 1 | a0001c0001t0003g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.119+6447C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040455 | ||||||
| chrX:38040460
|
C | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.119+6452C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040460 | ||||||
| chrX:38040461
|
C | G | 1 | a0001c0001t0005g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.119+6453C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040461 | ||||||
| chrX:38040585
|
C | T | 49 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.119+6577C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040585 | ||||||
| chrX:38040646
|
A | T | 13 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0237others(10): Show | 14 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(11): Show |
intron_variant | MODIFIER | c.119+6638A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040646 | ||||||
| chrX:38041074
|
A | G | 62 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(59): Show | 63 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.119+7066A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041074 | ||||||
| chrX:38041081
|
C | G | 92 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(89): Show | 94 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(91): Show |
intron_variant | MODIFIER | c.119+7073C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041081 | ||||||
| chrX:38041124
|
A | T | 53 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(50): Show | 53 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.119+7116A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041124 | ||||||
| chrX:38041243
|
C | T | 86 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(83): Show | 88 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.119+7235C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041243 | ||||||
| chrX:38041753
|
C | T | 7 | a0001c0004t0003g0230a0001c0004t0004g0232a0001c0004t0004g0233others(4): Show | 7 | HG02451.hp1 HG03195.hp2 HG03491.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+7745C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041753 | ||||||
| chrX:38041946
|
T | A | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.119+7938T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041946 | ||||||
| chrX:38041961
|
T | C | 3 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012 | 3 | HG02145.hp1 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.119+7953T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38041961 | ||||||
| chrX:38042110
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.119+8102A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042110 | ||||||
| chrX:38042205
|
T | G | 1 | a0001c0001t0001g0206 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.119+8197T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042205 | ||||||
| chrX:38042235
|
G | A | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.119+8227G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042235 | ||||||
| chrX:38042243
|
A | T | 1 | a0001c0001t0001g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.119+8235A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042243 | ||||||
| chrX:38042532
|
C | T | 1 | a0001c0001t0014g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.119+8524C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042532 | ||||||
| chrX:38042545
|
A | T | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.119+8537A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042545 | ||||||
| chrX:38042645
|
G | A | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.119+8637G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042645 | ||||||
| chrX:38042994
|
A | G | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.119+8986A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38042994 | ||||||
| chrX:38043002
|
TA | T | 1 | a0001c0001t0003g0106 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.119+8996delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043002 | |||||
| chrX:38043002
|
TAA | T | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.119+8995_119+8996d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043002 | ||||||
| chrX:38043283
|
A | G | 14 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(11): Show | 15 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.119+9275A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043283 | ||||||
| chrX:38043450
|
A | G | 4 | a0001c0001t0001g0117a0001c0001t0001g0126a0001c0001t0001g0135others(1): Show | 4 | HG02074.hp1 NA18946.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+9442A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043450 | ||||||
| chrX:38043577
|
C | A | 53 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(50): Show | 53 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.119+9569C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043577 | ||||||
| chrX:38043659
|
A | ATG | 2 | a0002c0003t0006g0024a0002c0003t0006g0025 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.119+9653_119+9654d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043659 | |||||
| chrX:38043659
|
A | G | 18 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(15): Show | 19 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.119+9651A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043659 | ||||||
| chrX:38043661
|
G | GTA | 9 | a0001c0001t0001g0148a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.119+9682_119+9683d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATA | 4 | a0001c0001t0001g0099a0001c0001t0001g0101a0001c0001t0001g0149others(1): Show | 4 | HG02129.hp1 HG02738.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+9680_119+9683d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATA | 3 | a0001c0001t0001g0120a0001c0001t0001g0226a0003c0005t0002g0056 | 3 | HG00735.hp2 NA19060.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.119+9678_119+9683d others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(1): Show |
4 | a0001c0001t0001g0072a0001c0001t0001g0080a0001c0004t0003g0230others(1): Show | 4 | HG02735.hp1 HG03540.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+9676_119+9683d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0001g0126a0001c0001t0001g0146a0002c0003t0002g0046 | 3 | HG02155.hp2 HG03098.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.119+9674_119+9683d others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(5): Show |
15 | a0001c0001t0001g0076a0001c0001t0001g0105a0001c0001t0001g0112others(12): Show | 16 | HG00544.hp1 HG00597.hp2 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.119+9672_119+9683d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(7): Show |
13 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0081others(10): Show | 13 | HG00621.hp1 HG00741.hp2 HG01952.hp1 others(10): Show |
intron_variant | MODIFIER | c.119+9670_119+9683d others(16): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(9): Show |
13 | a0001c0001t0001g0073a0001c0001t0001g0079a0001c0001t0001g0114others(10): Show | 13 | HG06807.hp1 NA18954.hp2 NA18960.hp1 others(10): Show |
intron_variant | MODIFIER | c.119+9668_119+9683d others(18): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(11): Show |
4 | a0001c0001t0001g0124a0001c0001t0001g0141a0001c0001t0001g0152others(1): Show | 4 | HG00673.hp1 NA18950.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+9666_119+9683d others(20): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(13): Show |
6 | a0001c0001t0001g0075a0001c0001t0001g0109a0001c0001t0001g0111others(3): Show | 6 | HG02004.hp1 HG02027.hp1 HG02083.hp1 others(3): Show |
intron_variant | MODIFIER | c.119+9664_119+9683d others(22): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(15): Show |
4 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0004t0004g0234others(1): Show | 4 | HG02451.hp1 HG03540.hp2 NA19055.hp1 others(1): Show |
intron_variant | MODIFIER | c.119+9662_119+9683d others(24): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(17): Show |
2 | a0001c0001t0001g0125a0006c0009t0001g0096 | 2 | HG03710.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.119+9660_119+9683d others(26): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTATATAT others(19): Show |
1 | a0001c0001t0001g0138 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.119+9658_119+9683d others(28): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
G | GTGTA | 5 | a0001c0002t0021g0020a0001c0004t0002g0026a0002c0003t0007g0021others(2): Show | 5 | HG02559.hp2 HG02809.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.119+9654_119+9655i others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
GTA | G | 42 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(39): Show | 42 | HG00558.hp2 HG00597.hp1 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.119+9682_119+9683d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043661
|
GTATA | G | 3 | a0001c0001t0001g0202a0001c0001t0003g0246a0002c0003t0004g0201 | 3 | HG00642.hp1 HG01496.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.119+9680_119+9683d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043661 | |||||
| chrX:38043662
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0006g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.119+9666_119+9695d others(32): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043662 | |||||
| chrX:38043663
|
A | G | 1 | a0003c0005t0002g0001 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.119+9655A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043663 | ||||||
| chrX:38043671
|
A | ATATATAT others(15): Show |
1 | a0003c0005t0004g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.119+9683_119+9684i others(24): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043671 | |||||
| chrX:38043674
|
T | TATATATA others(35): Show |
1 | a0001c0001t0001g0121 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.119+9683_119+9684i others(44): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043674 | |||||
| chrX:38043678
|
TATATATA others(7): Show |
T | 15 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(12): Show | 16 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.119+9682_119+9695d others(16): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043678 | |||||
| chrX:38043680
|
TATATATA others(5): Show |
T | 3 | a0001c0001t0005g0034a0001c0004t0002g0016a0003c0005t0002g0006 | 3 | HG01891.hp1 HG02886.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.119+9689_119+9700d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043680 | |||||
| chrX:38043682
|
TATATATA others(3): Show |
T | 26 | a0001c0001t0005g0048a0001c0001t0005g0053a0001c0001t0005g0054others(23): Show | 26 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.119+9684_119+9693d others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043682 | |||||
| chrX:38043684
|
TATATATA others(1): Show |
T | 8 | a0001c0002t0002g0029a0001c0002t0002g0043a0001c0002t0002g0240others(5): Show | 9 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(6): Show |
intron_variant | MODIFIER | c.119+9684_119+9691d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043684 | |||||
| chrX:38043686
|
TATATAC | T | 2 | a0001c0002t0002g0027a0001c0002t0002g0057 | 2 | HG03209.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.119+9684_119+9689d others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043686 | |||||
| chrX:38043688
|
T | TATATATA others(15): Show |
1 | a0001c0001t0004g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.119+9683_119+9684i others(24): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043688 | |||||
| chrX:38043688
|
TATAC | T | 7 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0143others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.119+9684_119+9687d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043688 | |||||
| chrX:38043690
|
T | TATATACA others(1): Show |
1 | a0002c0003t0004g0088 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.119+9683_119+9684i others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
T | TATATATA others(3): Show |
1 | a0002c0003t0004g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.119+9683_119+9684i others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
T | TATATATA others(7): Show |
10 | a0001c0001t0001g0086a0001c0001t0001g0095a0002c0003t0004g0002others(7): Show | 11 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.119+9683_119+9684i others(16): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
T | TATATATA others(9): Show |
4 | a0001c0002t0004g0091a0001c0004t0004g0092a0002c0003t0004g0087others(1): Show | 4 | HG01243.hp1 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.119+9683_119+9684i others(18): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.119+9683_119+9684i others(20): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
T | TATATATA others(13): Show |
1 | a0001c0002t0009g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.119+9683_119+9684i others(22): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043690
|
TAC | T | 3 | a0001c0002t0002g0047a0001c0002t0020g0045a0001c0004t0002g0049 | 3 | HG02886.hp2 HG03139.hp1 HG03669.hp1 |
intron_variant | MODIFIER | c.119+9684_119+9685d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043690 | |||||
| chrX:38043692
|
C | T | 22 | a0001c0002t0002g0051a0001c0002t0002g0058a0001c0002t0002g0059others(19): Show | 22 | HG01884.hp1 HG02055.hp1 HG02109.hp1 others(19): Show |
intron_variant | MODIFIER | c.119+9684C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043692 | ||||||
| chrX:38043702
|
T | C | 2 | a0001c0004t0006g0171a0001c0004t0023g0019 | 2 | HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.119+9694T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38043702 | ||||||
| chrX:38043702
|
T | TAC | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.119+9696_119+9697d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38043702 | |||||
| chrX:38044112
|
C | T | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.120-10101C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044112 | ||||||
| chrX:38044257
|
G | A | 2 | a0001c0001t0003g0200a0001c0001t0003g0246 | 2 | NA18943.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.120-9956G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044257 | ||||||
| chrX:38044285
|
G | A | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.120-9928G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044285 | ||||||
| chrX:38044405
|
T | G | 50 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.120-9808T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044405 | ||||||
| chrX:38044620
|
C | T | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-9593C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044620 | ||||||
| chrX:38044775
|
G | A | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.120-9438G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38044775 | ||||||
| chrX:38045149
|
G | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.120-9064G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045149 | ||||||
| chrX:38045272
|
C | T | 1 | a0001c0002t0002g0058 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.120-8941C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045272 | ||||||
| chrX:38045279
|
C | G | 1 | a0001c0002t0009g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.120-8934C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045279 | ||||||
| chrX:38045458
|
G | A | 6 | a0001c0001t0006g0033a0001c0004t0002g0049a0002c0003t0002g0044others(3): Show | 6 | HG01884.hp1 HG03041.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.120-8755G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045458 | ||||||
| chrX:38045461
|
T | TTTTTG | 1 | a0001c0002t0002g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.120-8732_120-8728d others(7): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38045461 | |||||
| chrX:38045462
|
T | C | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.120-8751T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045462 | ||||||
| chrX:38045466
|
G | GT | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.120-8743dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38045466 | |||||
| chrX:38045478
|
T | TC | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.120-8735_120-8734i others(3): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045478 | ||||||
| chrX:38045569
|
T | G | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.120-8644T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045569 | ||||||
| chrX:38045701
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.120-8512C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045701 | ||||||
| chrX:38045734
|
C | A | 1 | a0002c0003t0004g0201 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.120-8479C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045734 | ||||||
| chrX:38045861
|
A | G | 50 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.120-8352A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38045861 | ||||||
| chrX:38045882
|
T | TC | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.120-8329dupC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38045882 | |||||
| chrX:38046292
|
C | T | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.120-7921C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046292 | ||||||
| chrX:38046389
|
G | A | 111 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(108): Show | 114 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.120-7824G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046389 | ||||||
| chrX:38046403
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.120-7810C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046403 | ||||||
| chrX:38046628
|
T | C | 87 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(84): Show | 89 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(86): Show |
intron_variant | MODIFIER | c.120-7585T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046628 | ||||||
| chrX:38046850
|
T | C | 50 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.120-7363T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046850 | ||||||
| chrX:38046882
|
A | G | 111 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(108): Show | 114 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(111): Show |
intron_variant | MODIFIER | c.120-7331A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046882 | ||||||
| chrX:38046909
|
G | A | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-7304G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046909 | ||||||
| chrX:38046972
|
C | T | 1 | a0001c0002t0002g0050 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.120-7241C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046972 | ||||||
| chrX:38046989
|
G | A | 1 | a0001c0002t0009g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.120-7224G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38046989 | ||||||
| chrX:38047005
|
C | T | 12 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0237others(9): Show | 13 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.120-7208C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047005 | ||||||
| chrX:38047048
|
C | T | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-7165C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047048 | ||||||
| chrX:38047064
|
C | T | 3 | a0001c0001t0001g0151a0001c0004t0006g0171a0001c0004t0023g0019 | 3 | HG01934.hp1 HG02572.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.120-7149C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047064 | ||||||
| chrX:38047135
|
G | A | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-7078G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047135 | ||||||
| chrX:38047330
|
G | A | 1 | a0003c0005t0002g0006 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.120-6883G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047330 | ||||||
| chrX:38047383
|
A | G | 192 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(189): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(193): Show |
intron_variant | MODIFIER | c.120-6830A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047383 | ||||||
| chrX:38047422
|
G | A | 85 | a0001c0001t0002g0009a0001c0001t0005g0034a0001c0001t0005g0048others(82): Show | 87 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(84): Show |
intron_variant | MODIFIER | c.120-6791G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047422 | ||||||
| chrX:38047545
|
T | G | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-6668T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047545 | ||||||
| chrX:38047547
|
C | G | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-6666C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047547 | ||||||
| chrX:38047571
|
C | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0197 | 2 | NA18946.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.120-6642C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047571 | ||||||
| chrX:38047587
|
C | T | 1 | a0001c0001t0005g0034 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.120-6626C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047587 | ||||||
| chrX:38047828
|
C | T | 2 | a0001c0001t0003g0183a0001c0001t0003g0184 | 2 | NA18953.hp1 NA18999.hp2 |
intron_variant | MODIFIER | c.120-6385C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047828 | ||||||
| chrX:38047982
|
C | T | 1 | a0001c0002t0004g0078 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.120-6231C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047982 | ||||||
| chrX:38048180
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.120-6033C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048180 | ||||||
| chrX:38048191
|
CA | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.120-6012delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38048191 | |||||
| chrX:38048192
|
A | G | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.120-6021A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048192 | ||||||
| chrX:38048193
|
A | G | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.120-6020A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048193 | ||||||
| chrX:38048234
|
A | G | 12 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0237others(9): Show | 13 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.120-5979A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048234 | ||||||
| chrX:38048382
|
C | T | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.120-5831C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048382 | ||||||
| chrX:38048527
|
C | CA | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-5670dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38048527 | |||||
| chrX:38048527
|
CA | C | 70 | a0001c0001t0001g0072a0001c0001t0001g0086a0001c0001t0001g0095others(67): Show | 71 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.120-5670delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38048527 | |||||
| chrX:38048527
|
CAA | C | 1 | a0001c0002t0009g0084 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.120-5671_120-5670d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38048527 | |||||
| chrX:38048601
|
A | G | 2 | a0001c0001t0001g0122a0001c0001t0001g0140 | 2 | NA19009.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.120-5612A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048601 | ||||||
| chrX:38048603
|
G | A | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-5610G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048603 | ||||||
| chrX:38048626
|
A | G | 106 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(103): Show | 109 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.120-5587A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048626 | ||||||
| chrX:38048683
|
C | T | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-5530C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048683 | ||||||
| chrX:38048728
|
CAAATGA | C | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.120-5484_120-5479d others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048728 | ||||||
| chrX:38048736
|
T | G | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.120-5477T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048736 | ||||||
| chrX:38048737
|
A | G | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.120-5476A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048737 | ||||||
| chrX:38048746
|
C | G | 104 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(101): Show | 107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-5467C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048746 | ||||||
| chrX:38049036
|
A | C | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-5177A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049036 | ||||||
| chrX:38049364
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.120-4849C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049364 | ||||||
| chrX:38049374
|
A | G | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-4839A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049374 | ||||||
| chrX:38049474
|
A | G | 50 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.120-4739A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049474 | ||||||
| chrX:38049475
|
T | C | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.120-4738T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049475 | ||||||
| chrX:38049552
|
A | T | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-4661A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049552 | ||||||
| chrX:38049655
|
G | A | 8 | a0001c0002t0021g0020a0001c0004t0002g0026a0002c0003t0006g0024others(5): Show | 9 | HG01261.hp1 HG01496.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.120-4558G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049655 | ||||||
| chrX:38050018
|
A | G | 1 | a0001c0001t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.120-4195A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050018 | ||||||
| chrX:38050060
|
A | G | 1 | a0003c0005t0002g0001 | 2 | HG01261.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.120-4153A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050060 | ||||||
| chrX:38050122
|
A | G | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.120-4091A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050122 | ||||||
| chrX:38050288
|
G | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-3925G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050288 | ||||||
| chrX:38050358
|
A | G | 1 | a0001c0004t0002g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.120-3855A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050358 | ||||||
| chrX:38050425
|
G | C | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-3788G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050425 | ||||||
| chrX:38050631
|
C | T | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-3582C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050631 | ||||||
| chrX:38050657
|
G | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-3556G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050657 | ||||||
| chrX:38050796
|
T | C | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-3417T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050796 | ||||||
| chrX:38050797
|
T | C | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-3416T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050797 | ||||||
| chrX:38050813
|
G | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-3400G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050813 | ||||||
| chrX:38050857
|
G | C | 105 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(102): Show | 108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.120-3356G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050857 | ||||||
| chrX:38051231
|
A | G | 23 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(20): Show | 24 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.120-2982A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38051231 | ||||||
| chrX:38051334
|
TAA | T | 21 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(18): Show | 22 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.120-2876_120-2875d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38051334 | |||||
| chrX:38051345
|
T | G | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-2868T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38051345 | ||||||
| chrX:38051410
|
A | G | 1 | a0002c0003t0004g0094 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.120-2803A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38051410 | ||||||
| chrX:38051592
|
A | AG | 3 | a0001c0002t0002g0239a0001c0002t0002g0240a0001c0002t0002g0241 | 3 | HG02258.hp1 HG02622.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.120-2618dupG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38051592 | |||||
| chrX:38051623
|
C | A | 1 | a0001c0002t0002g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.120-2590C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38051623 | ||||||
| chrX:38051749
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.120-2464C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38051749 | ||||||
| chrX:38052068
|
G | A | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.120-2145G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052068 | ||||||
| chrX:38052146
|
G | T | 4 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0004t0002g0068others(1): Show | 4 | HG02280.hp1 HG02717.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.120-2067G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052146 | ||||||
| chrX:38052199
|
A | G | 6 | a0001c0004t0004g0232a0001c0004t0004g0233a0001c0004t0004g0234others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.120-2014A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052199 | ||||||
| chrX:38052381
|
A | G | 2 | a0001c0004t0003g0230a0003c0005t0003g0238 | 2 | HG03491.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.120-1832A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052381 | ||||||
| chrX:38052396
|
A | G | 1 | a0001c0001t0003g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.120-1817A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052396 | ||||||
| chrX:38052516
|
G | C | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-1697G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052516 | ||||||
| chrX:38052547
|
G | T | 13 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(10): Show | 13 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.120-1666G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052547 | ||||||
| chrX:38052725
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.120-1488G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052725 | ||||||
| chrX:38052753
|
C | T | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.120-1460C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052753 | ||||||
| chrX:38052968
|
T | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.120-1245T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38052968 | ||||||
| chrX:38053022
|
G | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-1191G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053022 | ||||||
| chrX:38053054
|
A | G | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.120-1159A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053054 | ||||||
| chrX:38053059
|
G | T | 18 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(15): Show | 19 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.120-1154G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053059 | ||||||
| chrX:38053583
|
G | C | 50 | a0001c0001t0005g0034a0001c0001t0005g0048a0001c0001t0005g0053others(47): Show | 50 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(47): Show |
intron_variant | MODIFIER | c.120-630G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053583 | ||||||
| chrX:38053958
|
A | C | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.120-255A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053958 | ||||||
| chrX:38054085
|
G | A | 1 | a0001c0001t0003g0210 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.120-128G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38054085 | ||||||
| chrX:38054198
|
C | T | 1 | a0001c0002t0002g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.120-15C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38054198 | ||||||
| chrX:38054463
|
CTG | C | 17 | a0001c0001t0001g0179a0001c0001t0001g0206a0001c0001t0003g0082others(14): Show | 17 | HG00609.hp1 HG02015.hp1 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.329+42_329+43delTG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38054463 | ||||||
| chrX:38054583
|
G | GGT | 2 | a0001c0001t0001g0111a0001c0001t0001g0138 | 2 | HG01943.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.329+184_329+185dup others(2): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054583 | |||||
| chrX:38054583
|
GGT | G | 156 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(153): Show | 159 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(156): Show |
intron_variant | MODIFIER | c.329+184_329+185del others(2): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054583 | |||||
| chrX:38054587
|
T | G | 6 | a0001c0004t0004g0232a0001c0004t0004g0233a0001c0004t0004g0234others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+165T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38054587 | ||||||
| chrX:38054611
|
T | TGA | 5 | a0001c0001t0001g0075a0001c0001t0001g0109a0001c0001t0001g0118others(2): Show | 5 | HG01074.hp1 HG02027.hp1 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.329+222_329+223dup others(2): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
T | TGAGA | 4 | a0001c0001t0001g0076a0001c0001t0001g0079a0001c0001t0001g0083others(1): Show | 4 | HG02080.hp1 HG02135.hp1 NA19006.hp1 others(1): Show |
intron_variant | MODIFIER | c.329+220_329+223dup others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
TGA | T | 54 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0179others(51): Show | 54 | HG00099.hp2 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.329+222_329+223del others(2): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
TGAGA | T | 2 | a0001c0001t0001g0081a0001c0001t0003g0144 | 2 | HG04204.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.329+220_329+223del others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
TGAGAGA | T | 5 | a0001c0001t0003g0159a0001c0002t0004g0091a0001c0004t0004g0092others(2): Show | 5 | HG00735.hp1 HG01255.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.329+218_329+223del others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
TGAGAGAG others(1): Show |
T | 65 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(62): Show | 66 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.329+216_329+223del others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054611
|
TGAGAGAG others(3): Show |
T | 35 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(32): Show | 37 | HG01261.hp1 HG01496.hp1 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.329+214_329+223del others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38054611 | |||||
| chrX:38054665
|
T | A | 103 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(100): Show | 106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.329+243T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38054665 | ||||||
| chrX:38054734
|
A | G | 12 | a0001c0002t0002g0027a0001c0002t0002g0029a0001c0002t0002g0237others(9): Show | 13 | HG02258.hp1 HG02280.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.329+312A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38054734 | ||||||
| chrX:38054818
|
C | T | 6 | a0001c0004t0004g0232a0001c0004t0004g0233a0001c0004t0004g0234others(3): Show | 6 | HG02451.hp1 HG03195.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.329+396C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38054818 | ||||||
| chrX:38055013
|
G | A | 104 | a0001c0001t0001g0086a0001c0001t0001g0095a0001c0001t0001g0169others(101): Show | 107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.329+591G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055013 | ||||||
| chrX:38055312
|
T | A | 1 | a0001c0002t0021g0020 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.329+890T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055312 | ||||||
| chrX:38055519
|
C | A | 1 | a0001c0002t0002g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.329+1097C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055519 | ||||||
| chrX:38055550
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.329+1128T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055550 | ||||||
| chrX:38055910
|
A | G | 1 | a0001c0002t0004g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.329+1488A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055910 | ||||||
| chrX:38055945
|
T | G | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.329+1523T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055945 | ||||||
| chrX:38055971
|
C | A | 45 | a0001c0001t0001g0095a0001c0001t0001g0169a0001c0001t0004g0168others(42): Show | 48 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(45): Show |
intron_variant | MODIFIER | c.329+1549C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38055971 | ||||||
| chrX:38056530
|
A | G | 1 | a0001c0001t0003g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.329+2108A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38056530 | ||||||
| chrX:38056669
|
A | G | 3 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | NA18950.hp1 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.329+2247A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38056669 | ||||||
| chrX:38056967
|
G | GC | 1 | a0001c0001t0005g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.329+2546dupC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38056967 | |||||
| chrX:38057124
|
A | T | 1 | a0001c0002t0002g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.329+2702A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057124 | ||||||
| chrX:38057315
|
A | G | 106 | a0001c0001t0002g0009a0001c0001t0004g0168a0001c0002t0002g0010others(103): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.329+2893A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057315 | ||||||
| chrX:38057431
|
A | G | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+3009A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057431 | ||||||
| chrX:38057480
|
G | A | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.329+3058G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057480 | ||||||
| chrX:38057614
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0166 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.329+3192C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057614 | ||||||
| chrX:38057702
|
A | G | 75 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(72): Show | 76 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.329+3280A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057702 | ||||||
| chrX:38057878
|
C | G | 12 | a0001c0004t0002g0004a0001c0004t0002g0236a0001c0004t0004g0232others(9): Show | 13 | HG01891.hp2 HG02451.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.329+3456C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057878 | ||||||
| chrX:38057913
|
T | C | 1 | a0001c0004t0002g0004 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.329+3491T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38057913 | ||||||
| chrX:38057989
|
A | AT | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329+3574dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38057989 | |||||
| chrX:38058357
|
T | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+3935T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38058357 | ||||||
| chrX:38058658
|
G | A | 13 | a0002c0003t0004g0002a0002c0003t0004g0085a0002c0003t0004g0087others(10): Show | 14 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.329+4236G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38058658 | ||||||
| chrX:38058693
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.329+4271A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38058693 | ||||||
| chrX:38058977
|
G | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.329+4555G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38058977 | ||||||
| chrX:38059108
|
T | C | 45 | a0001c0001t0001g0138a0001c0002t0002g0010a0001c0002t0002g0011others(42): Show | 45 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(42): Show |
intron_variant | MODIFIER | c.329+4686T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38059108 | ||||||
| chrX:38059268
|
C | T | 83 | a0001c0001t0001g0138a0001c0002t0002g0010a0001c0002t0002g0011others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.329+4846C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38059268 | ||||||
| chrX:38059316
|
G | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+4894G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38059316 | ||||||
| chrX:38059425
|
AG | A | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+5006delG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38059425 | |||||
| chrX:38059523
|
G | T | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.329+5101G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38059523 | ||||||
| chrX:38059695
|
TTTTG | T | 1 | a0001c0001t0003g0102 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.329+5290_329+5293d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38059695 | |||||
| chrX:38060053
|
G | GA | 1 | a0001c0001t0005g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.329+5631_329+5632i others(3): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060053 | ||||||
| chrX:38060136
|
ATACTT | A | 1 | a0003c0005t0002g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.329+5716_329+5720d others(7): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38060136 | |||||
| chrX:38060142
|
T | A | 1 | a0003c0005t0002g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.329+5720T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060142 | ||||||
| chrX:38060179
|
T | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+5757T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060179 | ||||||
| chrX:38060307
|
G | T | 2 | a0002c0003t0004g0085a0002c0003t0004g0093 | 2 | HG03688.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.329+5885G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060307 | ||||||
| chrX:38060319
|
C | T | 83 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.329+5897C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060319 | ||||||
| chrX:38060362
|
C | T | 1 | a0001c0004t0002g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.329+5940C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060362 | ||||||
| chrX:38060570
|
T | C | 31 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(28): Show | 32 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(29): Show |
intron_variant | MODIFIER | c.329+6148T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060570 | ||||||
| chrX:38060746
|
C | T | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0203 | 3 | HG00733.hp2 HG01106.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.329+6324C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060746 | ||||||
| chrX:38060771
|
T | A | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.329+6349T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060771 | ||||||
| chrX:38060777
|
G | A | 1 | a0001c0002t0002g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.329+6355G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060777 | ||||||
| chrX:38060828
|
A | C | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+6406A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38060828 | ||||||
| chrX:38060899
|
AC | A | 4 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0010g0017others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.329+6480delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38060899 | |||||
| chrX:38061022
|
T | A | 83 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.329+6600T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061022 | ||||||
| chrX:38061118
|
A | T | 3 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0134 | 3 | NA18950.hp1 NA18994.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.329+6696A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061118 | ||||||
| chrX:38061263
|
A | G | 76 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(73): Show | 77 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.329+6841A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061263 | ||||||
| chrX:38061285
|
TTGCAACT others(11): Show |
T | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.329+6866_329+6883d others(20): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38061285 | |||||
| chrX:38061367
|
GT | G | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+6949delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38061367 | |||||
| chrX:38061390
|
A | G | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+6968A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061390 | ||||||
| chrX:38061411
|
A | C | 4 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+6989A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061411 | ||||||
| chrX:38061422
|
A | G | 84 | a0001c0001t0003g0106a0001c0002t0002g0010a0001c0002t0002g0011others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.329+7000A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061422 | ||||||
| chrX:38061709
|
C | T | 80 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.329+7287C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061709 | ||||||
| chrX:38061715
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.329+7293G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061715 | ||||||
| chrX:38061802
|
T | G | 1 | a0001c0001t0004g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329+7380T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061802 | ||||||
| chrX:38061824
|
A | T | 4 | a0001c0002t0004g0091a0001c0004t0004g0092a0002c0003t0002g0243others(1): Show | 4 | HG01255.hp1 HG02451.hp2 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.329+7402A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061824 | ||||||
| chrX:38061832
|
A | G | 1 | a0001c0001t0004g0168 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.329+7410A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061832 | ||||||
| chrX:38061867
|
C | G | 1 | a0001c0001t0001g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.329+7445C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061867 | ||||||
| chrX:38061975
|
C | CT | 2 | a0003c0005t0002g0028a0003c0005t0003g0238 | 2 | HG02717.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.329+7563dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38061975 | |||||
| chrX:38061975
|
CT | C | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.329+7563delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38061975 | |||||
| chrX:38062002
|
C | G | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.329+7580C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062002 | ||||||
| chrX:38062058
|
C | A | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.329+7636C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062058 | ||||||
| chrX:38062102
|
G | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.329+7680G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062102 | ||||||
| chrX:38062154
|
G | A | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.329+7732G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062154 | ||||||
| chrX:38062267
|
G | A | 44 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(41): Show | 44 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.329+7845G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062267 | ||||||
| chrX:38062350
|
T | A | 10 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0245others(7): Show | 11 | HG01261.hp1 HG01496.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.329+7928T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062350 | ||||||
| chrX:38062672
|
A | T | 1 | a0001c0004t0006g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.329+8250A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062672 | ||||||
| chrX:38062719
|
T | A | 1 | a0001c0001t0012g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.329+8297T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062719 | ||||||
| chrX:38062849
|
ACCT | A | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.329+8431_329+8433d others(5): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38062849 | |||||
| chrX:38063089
|
G | GT | 43 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(40): Show | 43 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(40): Show |
intron_variant | MODIFIER | c.329+8677dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38063089 | |||||
| chrX:38063089
|
G | GTT | 1 | a0001c0002t0002g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.329+8676_329+8677d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38063089 | |||||
| chrX:38063787
|
AT | A | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-8256delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38063787 | |||||
| chrX:38063845
|
GC | G | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-8200delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38063845 | |||||
| chrX:38064058
|
CAT | C | 17 | a0001c0004t0004g0232a0001c0004t0004g0233a0001c0004t0004g0234others(14): Show | 18 | HG01261.hp1 HG01496.hp1 HG01891.hp2 others(15): Show |
intron_variant | MODIFIER | c.330-7980_330-7979d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38064058 | |||||
| chrX:38064065
|
A | ATG | 1 | a0001c0004t0002g0004 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.330-7981_330-7980i others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38064065 | |||||
| chrX:38064067
|
A | G | 2 | a0001c0004t0002g0004a0001c0004t0002g0242 | 3 | HG02723.hp1 HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.330-7980A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38064067 | ||||||
| chrX:38064067
|
ATG | A | 73 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(70): Show | 74 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(71): Show |
intron_variant | MODIFIER | c.330-7960_330-7959d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38064067 | |||||
| chrX:38064164
|
CA | C | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-7878delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38064164 | |||||
| chrX:38064225
|
G | A | 5 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0056others(2): Show | 6 | HG01261.hp1 HG01496.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-7822G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38064225 | ||||||
| chrX:38064419
|
AT | A | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-7624delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38064419 | |||||
| chrX:38064443
|
G | T | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.330-7604G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38064443 | ||||||
| chrX:38064558
|
G | C | 18 | a0001c0002t0004g0091a0001c0004t0004g0092a0002c0003t0002g0064others(15): Show | 19 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(16): Show |
intron_variant | MODIFIER | c.330-7489G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38064558 | ||||||
| chrX:38064589
|
A | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.330-7458A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38064589 | ||||||
| chrX:38065140
|
A | G | 44 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(41): Show | 44 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.330-6907A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065140 | ||||||
| chrX:38065179
|
A | G | 81 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(78): Show | 83 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(80): Show |
intron_variant | MODIFIER | c.330-6868A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065179 | ||||||
| chrX:38065225
|
A | G | 6 | a0001c0001t0001g0076a0001c0001t0001g0081a0001c0001t0001g0105others(3): Show | 6 | HG00741.hp2 HG02080.hp2 HG02135.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-6822A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065225 | ||||||
| chrX:38065307
|
CT | C | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-6735delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38065307 | |||||
| chrX:38065377
|
AT | A | 5 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0056others(2): Show | 6 | HG01261.hp1 HG01496.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.330-6667delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38065377 | |||||
| chrX:38065386
|
T | A | 88 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(85): Show | 89 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.330-6661T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065386 | ||||||
| chrX:38065774
|
G | A | 2 | a0003c0005t0002g0028a0003c0005t0003g0238 | 2 | HG02717.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.330-6273G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065774 | ||||||
| chrX:38065821
|
C | CG | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-6223dupG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38065821 | |||||
| chrX:38065821
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0003g0106 | 2 | HG03669.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.330-6226C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065821 | ||||||
| chrX:38065955
|
C | T | 1 | a0002c0003t0004g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.330-6092C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065955 | ||||||
| chrX:38065957
|
G | A | 5 | a0001c0001t0003g0153a0001c0001t0003g0155a0001c0001t0003g0183others(2): Show | 5 | HG03654.hp1 NA18955.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-6090G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38065957 | ||||||
| chrX:38066099
|
C | CA | 1 | a0001c0010t0005g0031 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.330-5939dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38066099 | |||||
| chrX:38066134
|
A | C | 1 | a0005c0007t0006g0065 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.330-5913A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066134 | ||||||
| chrX:38066250
|
C | A | 1 | a0001c0004t0004g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.330-5797C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066250 | ||||||
| chrX:38066499
|
A | G | 20 | a0001c0002t0004g0091a0002c0003t0002g0044a0002c0003t0002g0046others(17): Show | 21 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.330-5548A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066499 | ||||||
| chrX:38066745
|
A | C | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-5302A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066745 | ||||||
| chrX:38066759
|
T | C | 78 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(75): Show | 80 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(77): Show |
intron_variant | MODIFIER | c.330-5288T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066759 | ||||||
| chrX:38066768
|
A | G | 2 | a0001c0001t0003g0224a0001c0001t0003g0229 | 2 | HG00741.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.330-5279A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066768 | ||||||
| chrX:38066914
|
T | C | 58 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(55): Show | 59 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.330-5133T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066914 | ||||||
| chrX:38066994
|
G | A | 3 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0056 | 4 | HG01261.hp1 HG01496.hp1 HG02886.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-5053G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38066994 | ||||||
| chrX:38067054
|
G | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-4993G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067054 | ||||||
| chrX:38067253
|
A | G | 1 | a0001c0004t0004g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.330-4794A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067253 | ||||||
| chrX:38067255
|
G | C | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.330-4792G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067255 | ||||||
| chrX:38067272
|
T | C | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.330-4775T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067272 | ||||||
| chrX:38067382
|
C | CA | 34 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(31): Show | 36 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.330-4651dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38067382 | |||||
| chrX:38067382
|
CA | C | 2 | a0001c0001t0005g0067a0001c0010t0005g0031 | 2 | NA19083.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.330-4651delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38067382 | |||||
| chrX:38067387
|
A | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.330-4660A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067387 | ||||||
| chrX:38067404
|
G | A | 1 | a0001c0002t0002g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.330-4643G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067404 | ||||||
| chrX:38067922
|
A | G | 26 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(23): Show | 27 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.330-4125A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067922 | ||||||
| chrX:38067978
|
A | G | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.330-4069A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38067978 | ||||||
| chrX:38068291
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0104 | 2 | HG01192.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.330-3756G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38068291 | ||||||
| chrX:38068834
|
C | A | 5 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037others(2): Show | 5 | HG00544.hp2 HG00558.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.330-3213C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38068834 | ||||||
| chrX:38068834
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.330-3213C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38068834 | ||||||
| chrX:38068880
|
G | A | 26 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(23): Show | 27 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.330-3167G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38068880 | ||||||
| chrX:38068891
|
G | A | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.330-3156G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38068891 | ||||||
| chrX:38069467
|
C | T | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.330-2580C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069467 | ||||||
| chrX:38069676
|
A | G | 1 | a0001c0002t0002g0069 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.330-2371A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069676 | ||||||
| chrX:38069810
|
G | A | 2 | a0001c0001t0003g0207a0001c0001t0014g0177 | 2 | HG03831.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.330-2237G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069810 | ||||||
| chrX:38069844
|
C | A | 75 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(72): Show | 76 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.330-2203C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069844 | ||||||
| chrX:38069901
|
C | A | 1 | a0001c0004t0010g0018 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.330-2146C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069901 | ||||||
| chrX:38069960
|
G | T | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.330-2087G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069960 | ||||||
| chrX:38069962
|
A | G | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-2085A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38069962 | ||||||
| chrX:38070025
|
C | T | 35 | a0001c0002t0002g0012a0001c0002t0002g0029a0001c0002t0002g0035others(32): Show | 35 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(32): Show |
intron_variant | MODIFIER | c.330-2022C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070025 | ||||||
| chrX:38070527
|
C | A | 1 | a0001c0002t0002g0013 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.330-1520C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070527 | ||||||
| chrX:38070567
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.330-1480A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070567 | ||||||
| chrX:38070653
|
C | CTATTGAA | 1 | a0001c0004t0004g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.330-1393_330-1392i others(9): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38070653 | |||||
| chrX:38070699
|
A | G | 1 | a0001c0004t0004g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.330-1348A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070699 | ||||||
| chrX:38070705
|
C | G | 44 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(41): Show | 44 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.330-1342C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070705 | ||||||
| chrX:38070711
|
A | G | 1 | a0001c0001t0004g0195 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.330-1336A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070711 | ||||||
| chrX:38070811
|
C | A | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.330-1236C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070811 | ||||||
| chrX:38070882
|
T | C | 2 | a0001c0004t0004g0233a0001c0004t0004g0234 | 2 | HG02451.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.330-1165T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38070882 | ||||||
| chrX:38071054
|
G | GCAGT | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.330-993_330-992ins others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071054 | ||||||
| chrX:38071055
|
T | C | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.330-992T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071055 | ||||||
| chrX:38071055
|
T | TAGTC | 82 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(79): Show | 84 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.330-990_330-987dup others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | INFO_REALIGN_3_PRIME | chrX | 38071055 | |||||
| chrX:38071208
|
A | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.330-839A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071208 | ||||||
| chrX:38071389
|
C | G | 1 | a0001c0004t0002g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.330-658C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071389 | ||||||
| chrX:38071395
|
C | T | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-652C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071395 | ||||||
| chrX:38071452
|
C | T | 1 | a0002c0003t0004g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.330-595C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071452 | ||||||
| chrX:38071490
|
G | C | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.330-557G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071490 | ||||||
| chrX:38071589
|
T | C | 44 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(41): Show | 44 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.330-458T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38071589 | ||||||
| chrX:38072408
|
G | A | 2 | a0001c0002t0002g0237a0001c0002t0002g0240 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.445+246G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072408 | ||||||
| chrX:38072475
|
A | G | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.445+313A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072475 | ||||||
| chrX:38072583
|
T | C | 83 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.445+421T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072583 | ||||||
| chrX:38072605
|
T | C | 1 | a0001c0004t0003g0230 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.445+443T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072605 | ||||||
| chrX:38072796
|
G | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.445+634G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072796 | ||||||
| chrX:38072818
|
T | C | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.445+656T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072818 | ||||||
| chrX:38072863
|
G | C | 6 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.445+701G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38072863 | ||||||
| chrX:38073303
|
C | G | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.446-287C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38073303 | ||||||
| chrX:38073330
|
G | A | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.446-260G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 4/16 | chrX | 38073330 | ||||||
| chrX:38073877
|
T | C | 60 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(57): Show | 61 | HG00544.hp1 HG00597.hp2 HG00621.hp1 others(58): Show |
intron_variant | MODIFIER | c.554+179T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38073877 | ||||||
| chrX:38074100
|
T | A | 4 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0010g0017others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+402T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074100 | ||||||
| chrX:38074184
|
T | C | 5 | a0001c0001t0001g0095a0001c0001t0001g0108a0001c0001t0001g0118others(2): Show | 5 | HG00099.hp1 HG01074.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.554+486T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074184 | ||||||
| chrX:38074349
|
A | G | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.554+651A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074349 | ||||||
| chrX:38074448
|
A | T | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.554+750A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074448 | ||||||
| chrX:38074466
|
G | C | 1 | a0002c0003t0004g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.554+768G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074466 | ||||||
| chrX:38074573
|
C | G | 2 | a0001c0001t0003g0198a0001c0001t0003g0199 | 2 | NA18939.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.554+875C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074573 | ||||||
| chrX:38074708
|
T | A | 1 | a0001c0004t0004g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.554+1010T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074708 | ||||||
| chrX:38074719
|
C | G | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.554+1021C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38074719 | ||||||
| chrX:38074905
|
A | AAC | 4 | a0001c0001t0001g0141a0001c0001t0003g0159a0001c0001t0003g0175others(1): Show | 4 | HG00558.hp2 HG00673.hp1 HG00735.hp1 others(1): Show |
intron_variant | MODIFIER | c.554+1235_554+1236d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chrX | 38074905 | |||||
| chrX:38074905
|
AAC | A | 84 | a0001c0001t0001g0086a0001c0001t0001g0104a0001c0001t0003g0194others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.554+1235_554+1236d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chrX | 38074905 | |||||
| chrX:38074905
|
AACAC | A | 2 | a0001c0002t0002g0244a0003c0005t0002g0028 | 2 | HG02717.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.554+1233_554+1236d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chrX | 38074905 | |||||
| chrX:38074905
|
AACACACA others(1): Show |
A | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.554+1229_554+1236d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | INFO_REALIGN_3_PRIME | chrX | 38074905 | |||||
| chrX:38075117
|
G | A | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.554+1419G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075117 | ||||||
| chrX:38075123
|
G | A | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.554+1425G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075123 | ||||||
| chrX:38075206
|
C | T | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-1361C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075206 | ||||||
| chrX:38075387
|
A | C | 3 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0245 | 3 | HG02055.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.555-1180A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075387 | ||||||
| chrX:38075621
|
A | G | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.555-946A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075621 | ||||||
| chrX:38075769
|
G | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.555-798G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38075769 | ||||||
| chrX:38076104
|
T | A | 83 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.555-463T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38076104 | ||||||
| chrX:38076229
|
A | T | 1 | a0001c0001t0003g0246 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.555-338A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38076229 | ||||||
| chrX:38076523
|
G | T | 8 | a0002c0003t0004g0002a0002c0003t0004g0087a0002c0003t0004g0088others(5): Show | 9 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.555-44G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 5/16 | chrX | 38076523 | ||||||
| chrX:38076741
|
T | A | 83 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(80): Show | 85 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.689+40T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38076741 | ||||||
| chrX:38076868
|
A | T | 1 | a0001c0002t0002g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.689+167A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38076868 | ||||||
| chrX:38076935
|
T | C | 47 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(44): Show | 47 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.689+234T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38076935 | ||||||
| chrX:38077043
|
G | T | 1 | a0001c0001t0001g0124 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.689+342G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077043 | ||||||
| chrX:38077255
|
T | A | 1 | a0001c0001t0001g0119 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.689+554T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077255 | ||||||
| chrX:38077266
|
T | C | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689+565T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077266 | ||||||
| chrX:38077448
|
G | C | 102 | a0001c0001t0002g0009a0001c0001t0004g0168a0001c0002t0002g0010others(99): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.689+747G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077448 | ||||||
| chrX:38077568
|
T | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.689+867T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077568 | ||||||
| chrX:38077570
|
G | T | 7 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0002g0242others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.689+869G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077570 | ||||||
| chrX:38077661
|
G | GA | 8 | a0001c0001t0001g0203a0003c0005t0002g0001a0003c0005t0002g0006others(5): Show | 9 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.689+970dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38077661 | |||||
| chrX:38077661
|
GA | G | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.689+970delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38077661 | |||||
| chrX:38077738
|
CA | C | 1 | a0001c0001t0015g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.689+1040delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38077738 | |||||
| chrX:38077910
|
A | G | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.689+1209A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077910 | ||||||
| chrX:38077922
|
C | T | 1 | a0001c0001t0004g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.689+1221C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077922 | ||||||
| chrX:38078032
|
CA | C | 2 | a0001c0001t0001g0103a0001c0001t0001g0132 | 2 | NA18957.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.689+1340delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38078032 | |||||
| chrX:38078144
|
C | A | 1 | a0003c0005t0004g0161 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.689+1443C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078144 | ||||||
| chrX:38078153
|
C | T | 7 | a0001c0004t0002g0004a0001c0004t0004g0092a0001c0004t0004g0232others(4): Show | 8 | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+1452C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078153 | ||||||
| chrX:38078266
|
GT | G | 82 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(79): Show | 84 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.689+1577delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38078266 | |||||
| chrX:38078272
|
T | G | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.689+1571T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078272 | ||||||
| chrX:38078291
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.689+1590C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078291 | ||||||
| chrX:38078304
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.689+1603G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078304 | ||||||
| chrX:38078386
|
G | A | 1 | a0001c0004t0023g0019 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.689+1685G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078386 | ||||||
| chrX:38078540
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.689+1839G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078540 | ||||||
| chrX:38078576
|
G | GA | 2 | a0001c0002t0002g0070a0001c0002t0002g0071 | 2 | HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.689+1885dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38078576 | |||||
| chrX:38078693
|
G | A | 8 | a0001c0004t0002g0004a0001c0004t0002g0236a0001c0004t0004g0092others(5): Show | 9 | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.689+1992G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078693 | ||||||
| chrX:38078702
|
T | G | 1 | a0001c0001t0001g0157 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.689+2001T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078702 | ||||||
| chrX:38078750
|
A | G | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.689+2049A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078750 | ||||||
| chrX:38078791
|
G | A | 1 | a0001c0001t0001g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.689+2090G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078791 | ||||||
| chrX:38078844
|
G | T | 1 | a0007c0011t0001g0131 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.689+2143G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078844 | ||||||
| chrX:38079020
|
T | C | 25 | a0001c0002t0002g0244a0002c0003t0002g0044a0002c0003t0002g0046others(22): Show | 26 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.689+2319T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079020 | ||||||
| chrX:38079070
|
A | G | 3 | a0001c0001t0008g0097a0001c0001t0008g0098a0001c0001t0019g0041 | 3 | HG01952.hp1 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.689+2369A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079070 | ||||||
| chrX:38079249
|
C | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.689+2548C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079249 | ||||||
| chrX:38079255
|
G | A | 2 | a0001c0002t0002g0038a0001c0002t0004g0078 | 2 | HG02523.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.689+2554G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079255 | ||||||
| chrX:38079273
|
TC | T | 1 | a0001c0001t0015g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.689+2574delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38079273 | |||||
| chrX:38079301
|
G | A | 2 | a0001c0002t0002g0237a0001c0002t0002g0240 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.689+2600G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079301 | ||||||
| chrX:38079489
|
T | C | 1 | a0001c0002t0002g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.689+2788T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079489 | ||||||
| chrX:38079953
|
T | G | 25 | a0001c0002t0002g0244a0002c0003t0002g0044a0002c0003t0002g0046others(22): Show | 26 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(23): Show |
intron_variant | MODIFIER | c.689+3252T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38079953 | ||||||
| chrX:38080034
|
A | G | 2 | a0001c0001t0003g0214a0001c0001t0003g0222 | 2 | HG02071.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.689+3333A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38080034 | ||||||
| chrX:38080434
|
TC | T | 1 | a0001c0001t0015g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.689+3735delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38080434 | |||||
| chrX:38080487
|
A | G | 84 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.689+3786A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38080487 | ||||||
| chrX:38080548
|
TC | T | 1 | a0001c0001t0015g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.689+3849delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38080548 | |||||
| chrX:38080617
|
GC | G | 1 | a0001c0001t0015g0165 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.689+3920delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38080617 | |||||
| chrX:38080992
|
A | C | 4 | a0001c0002t0002g0012a0001c0002t0002g0029a0001c0002t0002g0069others(1): Show | 4 | HG02451.hp2 HG02922.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.689+4291A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38080992 | ||||||
| chrX:38081000
|
T | TA | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.689+4306dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38081000 | |||||
| chrX:38081017
|
G | A | 7 | a0001c0004t0002g0004a0001c0004t0004g0092a0001c0004t0004g0232others(4): Show | 8 | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.689+4316G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081017 | ||||||
| chrX:38081066
|
G | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.689+4365G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081066 | ||||||
| chrX:38081164
|
C | CT | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.689+4470dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38081164 | |||||
| chrX:38081217
|
C | T | 1 | a0001c0001t0003g0082 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.689+4516C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081217 | ||||||
| chrX:38081222
|
G | A | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.689+4521G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081222 | ||||||
| chrX:38081426
|
A | G | 6 | a0001c0002t0002g0027a0001c0002t0002g0070a0001c0002t0002g0071others(3): Show | 6 | HG02055.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.689+4725A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081426 | ||||||
| chrX:38081576
|
T | C | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.689+4875T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081576 | ||||||
| chrX:38081891
|
C | T | 1 | a0009c0012t0003g0190 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.689+5190C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38081891 | ||||||
| chrX:38082027
|
C | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.689+5326C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082027 | ||||||
| chrX:38082111
|
G | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.689+5410G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082111 | ||||||
| chrX:38082279
|
C | A | 100 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(97): Show | 103 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(100): Show |
intron_variant | MODIFIER | c.689+5578C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082279 | ||||||
| chrX:38082348
|
T | C | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.689+5647T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082348 | ||||||
| chrX:38082478
|
T | C | 84 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(81): Show | 86 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(83): Show |
intron_variant | MODIFIER | c.689+5777T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082478 | ||||||
| chrX:38082533
|
G | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.689+5832G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082533 | ||||||
| chrX:38082545
|
G | A | 27 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.689+5844G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082545 | ||||||
| chrX:38082977
|
T | C | 1 | a0001c0002t0002g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.689+6276T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38082977 | ||||||
| chrX:38083034
|
G | C | 1 | a0001c0001t0001g0108 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.689+6333G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083034 | ||||||
| chrX:38083178
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.690-6268C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083178 | ||||||
| chrX:38083249
|
T | C | 2 | a0002c0003t0006g0024a0002c0003t0006g0025 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.690-6197T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083249 | ||||||
| chrX:38083453
|
G | A | 76 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(73): Show | 77 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.690-5993G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083453 | ||||||
| chrX:38083485
|
T | C | 1 | a0001c0001t0004g0003 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.690-5961T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083485 | ||||||
| chrX:38083638
|
T | C | 5 | a0001c0002t0002g0047a0001c0002t0002g0059a0001c0002t0002g0060others(2): Show | 5 | HG02109.hp1 HG02886.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-5808T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083638 | ||||||
| chrX:38083663
|
C | A | 6 | a0002c0003t0002g0243a0002c0003t0006g0024a0002c0003t0006g0025others(3): Show | 6 | HG02559.hp2 HG02630.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-5783C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083663 | ||||||
| chrX:38083663
|
C | T | 2 | a0001c0001t0001g0172a0001c0001t0001g0173 | 2 | HG00733.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.690-5783C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083663 | ||||||
| chrX:38083738
|
T | C | 1 | a0001c0001t0001g0073 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.690-5708T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083738 | ||||||
| chrX:38083757
|
A | T | 102 | a0001c0001t0002g0009a0001c0001t0004g0168a0001c0002t0002g0010others(99): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.690-5689A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083757 | ||||||
| chrX:38083773
|
C | CGTGTGTG others(3): Show |
2 | a0001c0002t0002g0219a0001c0002t0002g0220 | 2 | HG01175.hp2 HG01256.hp1 |
intron_variant | MODIFIER | c.690-5673_690-5672i others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083773 | ||||||
| chrX:38083773
|
C | CGTGTGTG others(5): Show |
1 | a0001c0002t0002g0215 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.690-5673_690-5672i others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083773 | ||||||
| chrX:38083774
|
A | ATG | 5 | a0001c0004t0002g0004a0002c0003t0002g0064a0002c0003t0004g0167others(2): Show | 6 | HG01255.hp1 HG03195.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.690-5638_690-5637d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTG | 16 | a0002c0003t0002g0243a0002c0003t0004g0002a0002c0003t0004g0085others(13): Show | 17 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(14): Show |
intron_variant | MODIFIER | c.690-5640_690-5637d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTG | 11 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(8): Show | 11 | HG01884.hp1 HG01884.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.690-5642_690-5637d others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTGT others(1): Show |
30 | a0001c0001t0002g0009a0001c0002t0002g0010a0001c0002t0002g0011others(27): Show | 30 | HG00544.hp2 HG00597.hp1 HG00639.hp2 others(27): Show |
intron_variant | MODIFIER | c.690-5644_690-5637d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTGT others(3): Show |
6 | a0001c0002t0002g0057a0001c0002t0002g0241a0001c0002t0020g0045others(3): Show | 6 | HG02280.hp1 HG02622.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.690-5646_690-5637d others(12): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTGT others(5): Show |
4 | a0001c0001t0004g0168a0001c0002t0002g0036a0001c0002t0004g0091others(1): Show | 4 | HG00558.hp1 HG02451.hp2 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.690-5648_690-5637d others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTGT others(7): Show |
11 | a0001c0002t0002g0012a0001c0002t0002g0027a0001c0002t0002g0029others(8): Show | 11 | HG02109.hp1 HG02886.hp2 HG02922.hp1 others(8): Show |
intron_variant | MODIFIER | c.690-5650_690-5637d others(16): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | ATGTGTGT others(9): Show |
1 | a0001c0002t0002g0240 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.690-5652_690-5637d others(18): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
A | G | 3 | a0001c0002t0002g0215a0001c0002t0002g0219a0001c0002t0002g0220 | 3 | HG01175.hp2 HG01256.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.690-5672A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083774 | ||||||
| chrX:38083774
|
ATG | A | 28 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0075others(25): Show | 28 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(25): Show |
intron_variant | MODIFIER | c.690-5638_690-5637d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
ATGTG | A | 109 | a0001c0001t0001g0072a0001c0001t0001g0076a0001c0001t0001g0081others(106): Show | 110 | HG00544.hp1 HG00558.hp2 HG00597.hp2 others(107): Show |
intron_variant | MODIFIER | c.690-5640_690-5637d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
ATGTGTG | A | 5 | a0001c0001t0003g0155a0001c0004t0004g0233a0001c0004t0004g0234others(2): Show | 5 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.690-5642_690-5637d others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083774
|
ATGTGTGT others(1): Show |
A | 1 | a0001c0004t0002g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.690-5644_690-5637d others(10): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083774 | |||||
| chrX:38083809
|
T | TGTGTGTG | 1 | a0001c0002t0002g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.690-5637_690-5636i others(9): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083809 | ||||||
| chrX:38083809
|
T | TGTGTGTG others(10): Show |
1 | a0001c0002t0002g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.690-5637_690-5636i others(19): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38083809 | ||||||
| chrX:38083835
|
A | AAT | 75 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(72): Show | 76 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(73): Show |
intron_variant | MODIFIER | c.690-5595_690-5594d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083835 | |||||
| chrX:38083835
|
A | AATAT | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.690-5597_690-5594d others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38083835 | |||||
| chrX:38084019
|
C | T | 2 | a0001c0001t0001g0110a0001c0001t0001g0145 | 2 | HG01099.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.690-5427C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38084019 | ||||||
| chrX:38084201
|
G | A | 2 | a0001c0001t0001g0110a0001c0001t0001g0145 | 2 | HG01099.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.690-5245G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38084201 | ||||||
| chrX:38084397
|
G | A | 1 | a0001c0004t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.690-5049G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38084397 | ||||||
| chrX:38084710
|
G | A | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.690-4736G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38084710 | ||||||
| chrX:38084717
|
A | AC | 157 | a0001c0001t0001g0072a0001c0001t0001g0130a0001c0001t0001g0172others(154): Show | 160 | HG00544.hp2 HG00558.hp1 HG00558.hp2 others(157): Show |
intron_variant | MODIFIER | c.690-4729_690-4728i others(3): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38084717 | ||||||
| chrX:38085071
|
C | T | 1 | a0001c0004t0006g0171 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.690-4375C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085071 | ||||||
| chrX:38085137
|
TA | T | 2 | a0001c0004t0002g0004a0001c0004t0002g0236 | 3 | HG03195.hp1 HG03486.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.690-4298delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | INFO_REALIGN_3_PRIME | chrX | 38085137 | |||||
| chrX:38085340
|
A | G | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-4106A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085340 | ||||||
| chrX:38085475
|
T | G | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-3971T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085475 | ||||||
| chrX:38085611
|
A | T | 49 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.690-3835A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085611 | ||||||
| chrX:38085839
|
T | G | 49 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(46): Show | 49 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(46): Show |
intron_variant | MODIFIER | c.690-3607T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085839 | ||||||
| chrX:38085845
|
CT | C | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.690-3600delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38085845 | ||||||
| chrX:38086632
|
T | C | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.690-2814T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086632 | ||||||
| chrX:38086699
|
T | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.690-2747T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086699 | ||||||
| chrX:38086711
|
A | G | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.690-2735A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086711 | ||||||
| chrX:38086730
|
G | A | 2 | a0001c0001t0001g0114a0001c0001t0001g0162 | 2 | NA18966.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.690-2716G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086730 | ||||||
| chrX:38086774
|
A | G | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.690-2672A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086774 | ||||||
| chrX:38086812
|
C | T | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.690-2634C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086812 | ||||||
| chrX:38086841
|
A | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.690-2605A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38086841 | ||||||
| chrX:38087138
|
G | A | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.690-2308G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087138 | ||||||
| chrX:38087206
|
T | G | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.690-2240T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087206 | ||||||
| chrX:38087259
|
G | A | 1 | a0001c0001t0001g0202 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.690-2187G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087259 | ||||||
| chrX:38087354
|
T | A | 4 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0010g0017others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.690-2092T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087354 | ||||||
| chrX:38087356
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.690-2090T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087356 | ||||||
| chrX:38087711
|
A | T | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.690-1735A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087711 | ||||||
| chrX:38087895
|
G | A | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.690-1551G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38087895 | ||||||
| chrX:38088288
|
A | G | 81 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.690-1158A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38088288 | ||||||
| chrX:38088352
|
C | T | 1 | a0001c0001t0001g0133 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.690-1094C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38088352 | ||||||
| chrX:38088462
|
C | A | 1 | a0001c0002t0002g0036 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.690-984C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38088462 | ||||||
| chrX:38088507
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.690-939C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38088507 | ||||||
| chrX:38089087
|
A | G | 2 | a0001c0001t0003g0223a0001c0001t0014g0177 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.690-359A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38089087 | ||||||
| chrX:38089379
|
A | T | 1 | a0001c0004t0004g0092 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.690-67A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38089379 | ||||||
| chrX:38089866
|
C | G | 8 | a0002c0003t0004g0002a0002c0003t0004g0087a0002c0003t0004g0088others(5): Show | 9 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.831+279C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38089866 | ||||||
| chrX:38089867
|
G | T | 1 | a0001c0004t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.831+280G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38089867 | ||||||
| chrX:38090110
|
T | C | 80 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.831+523T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38090110 | ||||||
| chrX:38090283
|
T | A | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.831+696T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38090283 | ||||||
| chrX:38090316
|
C | A | 3 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0245 | 3 | HG02055.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.831+729C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38090316 | ||||||
| chrX:38090873
|
G | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.831+1286G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38090873 | ||||||
| chrX:38091121
|
C | G | 2 | a0001c0001t0001g0113a0001c0001t0001g0121 | 2 | NA18990.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.831+1534C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091121 | ||||||
| chrX:38091200
|
T | C | 9 | a0001c0004t0004g0092a0001c0004t0004g0232a0003c0005t0002g0001others(6): Show | 10 | HG01261.hp1 HG01496.hp1 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.831+1613T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091200 | ||||||
| chrX:38091234
|
G | A | 1 | a0001c0001t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.831+1647G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091234 | ||||||
| chrX:38091518
|
G | T | 1 | a0001c0002t0002g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.831+1931G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091518 | ||||||
| chrX:38091533
|
C | CT | 102 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(99): Show | 105 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(102): Show |
intron_variant | MODIFIER | c.831+1946_831+1947i others(3): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091533 | ||||||
| chrX:38091555
|
A | T | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00544.hp2 HG00558.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.831+1968A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091555 | ||||||
| chrX:38091703
|
C | T | 1 | a0001c0001t0003g0224 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.831+2116C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091703 | ||||||
| chrX:38091898
|
G | A | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.831+2311G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38091898 | ||||||
| chrX:38092009
|
A | G | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.832-2286A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38092009 | ||||||
| chrX:38092198
|
T | A | 1 | a0001c0001t0005g0063 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.832-2097T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38092198 | ||||||
| chrX:38092684
|
G | A | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.832-1611G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38092684 | ||||||
| chrX:38092714
|
C | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.832-1581C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38092714 | ||||||
| chrX:38092956
|
A | T | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.832-1339A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38092956 | ||||||
| chrX:38093125
|
C | G | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.832-1170C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093125 | ||||||
| chrX:38093214
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.832-1081G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093214 | ||||||
| chrX:38093270
|
A | T | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.832-1025A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093270 | ||||||
| chrX:38093318
|
A | T | 1 | a0002c0003t0004g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.832-977A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093318 | ||||||
| chrX:38093528
|
G | T | 1 | a0001c0001t0004g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.832-767G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093528 | ||||||
| chrX:38093584
|
C | T | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.832-711C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093584 | ||||||
| chrX:38093589
|
C | A | 1 | a0001c0001t0001g0123 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.832-706C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093589 | ||||||
| chrX:38093603
|
C | A | 1 | a0002c0003t0004g0094 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.832-692C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | chrX | 38093603 | ||||||
| chrX:38094265
|
A | AT | 1 | a0002c0003t0004g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.832-23dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 7/16 | INFO_REALIGN_3_PRIME | chrX | 38094265 | |||||
| chrX:38094550
|
T | C | 1 | a0001c0001t0004g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.961+126T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38094550 | ||||||
| chrX:38094903
|
A | G | 1 | a0002c0003t0004g0167 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.961+479A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38094903 | ||||||
| chrX:38094985
|
G | C | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.961+561G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38094985 | ||||||
| chrX:38095175
|
C | T | 1 | a0001c0004t0002g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.961+751C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38095175 | ||||||
| chrX:38095176
|
C | G | 1 | a0001c0004t0002g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.961+752C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38095176 | ||||||
| chrX:38095253
|
T | A | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.961+829T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38095253 | ||||||
| chrX:38095769
|
G | GT | 37 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(34): Show | 39 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(36): Show |
intron_variant | MODIFIER | c.962-356dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chrX | 38095769 | |||||
| chrX:38095769
|
G | GTT | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.962-357_962-356dup others(2): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chrX | 38095769 | |||||
| chrX:38095769
|
GT | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.962-356delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | INFO_REALIGN_3_PRIME | chrX | 38095769 | |||||
| chrX:38096083
|
T | C | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.962-51T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 8/16 | chrX | 38096083 | ||||||
| chrX:38096426
|
T | A | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062+192T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096426 | ||||||
| chrX:38096503
|
C | G | 1 | a0001c0001t0003g0228 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1062+269C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096503 | ||||||
| chrX:38096514
|
A | T | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1062+280A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096514 | ||||||
| chrX:38096666
|
CATTTCTA | C | 2 | a0002c0003t0006g0024a0002c0003t0006g0025 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1062+433_1062+439d others(9): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096666 | ||||||
| chrX:38096674
|
G | C | 2 | a0002c0003t0006g0024a0002c0003t0006g0025 | 2 | HG02630.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.1062+440G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096674 | ||||||
| chrX:38096719
|
C | A | 1 | a0001c0002t0002g0036 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1062+485C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096719 | ||||||
| chrX:38096743
|
T | G | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1062+509T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096743 | ||||||
| chrX:38096768
|
C | T | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062+534C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096768 | ||||||
| chrX:38096878
|
A | C | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1062+644A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096878 | ||||||
| chrX:38096880
|
T | C | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1062+646T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096880 | ||||||
| chrX:38096949
|
C | T | 1 | a0001c0001t0003g0129 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1062+715C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096949 | ||||||
| chrX:38097096
|
G | GA | 1 | a0001c0002t0004g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1062+867dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38097096 | |||||
| chrX:38097188
|
G | A | 1 | a0001c0002t0002g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1062+954G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097188 | ||||||
| chrX:38097240
|
A | C | 4 | a0001c0001t0003g0194a0001c0001t0003g0200a0001c0001t0003g0246others(1): Show | 4 | HG02698.hp1 NA18943.hp1 NA18964.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+1006A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097240 | ||||||
| chrX:38097423
|
T | C | 2 | a0003c0005t0002g0006a0003c0005t0002g0028 | 2 | HG02717.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.1062+1189T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097423 | ||||||
| chrX:38097504
|
T | A | 1 | a0002c0003t0004g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1062+1270T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097504 | ||||||
| chrX:38097659
|
C | G | 1 | a0001c0001t0001g0095 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1062+1425C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097659 | ||||||
| chrX:38097847
|
A | G | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1062+1613A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097847 | ||||||
| chrX:38097880
|
G | GA | 1 | a0002c0003t0004g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1062+1660dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38097880 | |||||
| chrX:38097880
|
GA | G | 3 | a0001c0001t0003g0189a0001c0008t0004g0160a0002c0003t0004g0090 | 3 | HG03490.hp1 NA18522.hp1 NA19072.hp1 |
intron_variant | MODIFIER | c.1062+1660delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38097880 | |||||
| chrX:38097894
|
A | G | 1 | a0002c0003t0004g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1062+1660A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38097894 | ||||||
| chrX:38098128
|
G | A | 4 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0010g0017others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.1062+1894G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098128 | ||||||
| chrX:38098141
|
T | C | 4 | a0001c0004t0002g0007a0001c0004t0002g0008a0001c0004t0002g0026others(1): Show | 4 | HG02622.hp2 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1062+1907T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098141 | ||||||
| chrX:38098189
|
G | A | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+1955G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098189 | ||||||
| chrX:38098243
|
C | T | 1 | a0001c0001t0001g0113 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.1062+2009C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098243 | ||||||
| chrX:38098271
|
G | A | 1 | a0002c0003t0004g0002 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1062+2037G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098271 | ||||||
| chrX:38098465
|
C | T | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1062+2231C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098465 | ||||||
| chrX:38098625
|
G | A | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1062+2391G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098625 | ||||||
| chrX:38098644
|
T | C | 14 | a0001c0001t0001g0130a0001c0001t0001g0185a0001c0001t0003g0082others(11): Show | 14 | HG00609.hp1 HG02015.hp1 HG02523.hp2 others(11): Show |
intron_variant | MODIFIER | c.1062+2410T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098644 | ||||||
| chrX:38098970
|
T | C | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1062+2736T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098970 | ||||||
| chrX:38098983
|
T | A | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1062+2749T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098983 | ||||||
| chrX:38098990
|
C | T | 104 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(101): Show | 107 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(104): Show |
intron_variant | MODIFIER | c.1062+2756C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38098990 | ||||||
| chrX:38099237
|
T | C | 5 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0001g0077others(2): Show | 5 | HG00621.hp1 NA18612.hp1 NA18986.hp1 others(2): Show |
intron_variant | MODIFIER | c.1062+3003T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38099237 | ||||||
| chrX:38099430
|
G | A | 1 | a0001c0002t0004g0127 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1063-2912G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38099430 | ||||||
| chrX:38099863
|
G | A | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1063-2479G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38099863 | ||||||
| chrX:38099984
|
G | A | 1 | a0001c0001t0001g0204 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1063-2358G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38099984 | ||||||
| chrX:38100172
|
A | C | 1 | a0001c0002t0002g0043 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1063-2170A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38100172 | ||||||
| chrX:38100194
|
C | A | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063-2148C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38100194 | ||||||
| chrX:38100417
|
A | T | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1063-1925A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38100417 | ||||||
| chrX:38100445
|
C | T | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1063-1897C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38100445 | ||||||
| chrX:38100610
|
T | A | 4 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015others(1): Show | 4 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1063-1732T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38100610 | ||||||
| chrX:38101138
|
G | A | 106 | a0001c0001t0002g0009a0001c0001t0004g0168a0001c0002t0002g0010others(103): Show | 109 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(106): Show |
intron_variant | MODIFIER | c.1063-1204G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101138 | ||||||
| chrX:38101379
|
C | T | 7 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1063-963C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101379 | ||||||
| chrX:38101600
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1063-742A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101600 | ||||||
| chrX:38101649
|
ATG | A | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1063-681_1063-680d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101649 | |||||
| chrX:38101681
|
GTA | G | 7 | a0001c0004t0002g0016a0001c0004t0002g0068a0001c0004t0002g0242others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063-651_1063-650d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101681 | |||||
| chrX:38101683
|
A | G | 1 | a0001c0004t0002g0004 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1063-659A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101683 | ||||||
| chrX:38101824
|
C | CAA | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1063-506_1063-505d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101824 | |||||
| chrX:38101824
|
CA | C | 86 | a0001c0001t0001g0125a0001c0001t0001g0126a0001c0001t0001g0135others(83): Show | 88 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(85): Show |
intron_variant | MODIFIER | c.1063-505delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101824 | |||||
| chrX:38101824
|
CAA | C | 6 | a0001c0002t0004g0176a0003c0005t0002g0001a0003c0005t0002g0006others(3): Show | 7 | HG00597.hp1 HG01261.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063-506_1063-505d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101824 | |||||
| chrX:38101964
|
AGT | A | 1 | a0001c0002t0002g0027 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1063-363_1063-362d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38101964 | |||||
| chrX:38101978
|
T | C | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1063-364T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101978 | ||||||
| chrX:38101994
|
C | T | 6 | a0003c0005t0002g0001a0003c0005t0002g0006a0003c0005t0002g0028others(3): Show | 7 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.1063-348C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101994 | ||||||
| chrX:38102080
|
A | G | 1 | a0001c0002t0020g0045 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1063-262A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38102080 | ||||||
| chrX:38102141
|
AC | A | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1063-196delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38102141 | |||||
| chrX:38102259
|
TGAAA | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1063-77_1063-74del others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | INFO_REALIGN_3_PRIME | chrX | 38102259 | |||||
| chrX:38102295
|
A | G | 4 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1063-47A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38102295 | ||||||
| chrX:38102545
|
A | G | 1 | a0002c0003t0004g0170 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1155+111A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102545 | ||||||
| chrX:38102700
|
C | A | 1 | a0001c0001t0004g0187 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1155+266C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102700 | ||||||
| chrX:38102709
|
A | G | 4 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1155+275A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102709 | ||||||
| chrX:38102757
|
T | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1155+323T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102757 | ||||||
| chrX:38102886
|
A | T | 80 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1155+452A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102886 | ||||||
| chrX:38102976
|
T | C | 1 | a0006c0009t0001g0096 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1155+542T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38102976 | ||||||
| chrX:38103119
|
C | A | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1155+685C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38103119 | ||||||
| chrX:38103194
|
C | T | 5 | a0001c0001t0003g0153a0001c0001t0003g0155a0001c0001t0003g0183others(2): Show | 5 | HG03654.hp1 NA18955.hp1 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.1155+760C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38103194 | ||||||
| chrX:38103772
|
T | G | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1155+1338T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38103772 | ||||||
| chrX:38103837
|
C | A | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1155+1403C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38103837 | ||||||
| chrX:38104196
|
T | C | 1 | a0001c0001t0001g0134 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.1155+1762T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38104196 | ||||||
| chrX:38104373
|
C | T | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1155+1939C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38104373 | ||||||
| chrX:38104596
|
C | A | 3 | a0001c0002t0002g0013a0001c0002t0002g0014a0001c0002t0002g0015 | 3 | HG01884.hp2 HG02109.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.1156-1997C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38104596 | ||||||
| chrX:38104835
|
T | A | 1 | a0001c0001t0005g0048 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1156-1758T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38104835 | ||||||
| chrX:38104911
|
G | A | 80 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(77): Show | 81 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(78): Show |
intron_variant | MODIFIER | c.1156-1682G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38104911 | ||||||
| chrX:38105160
|
A | G | 2 | a0001c0001t0002g0009a0001c0001t0004g0168 | 2 | HG03130.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1156-1433A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105160 | ||||||
| chrX:38105357
|
G | A | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1156-1236G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105357 | ||||||
| chrX:38105370
|
A | T | 1 | a0001c0001t0014g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1156-1223A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105370 | ||||||
| chrX:38105435
|
A | G | 1 | a0003c0005t0002g0028 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1156-1158A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105435 | ||||||
| chrX:38105568
|
A | AG | 5 | a0001c0004t0002g0007a0001c0004t0002g0008a0001c0004t0002g0026others(2): Show | 5 | HG02622.hp2 HG03139.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1156-1020dupG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chrX | 38105568 | |||||
| chrX:38105694
|
A | G | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1156-899A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105694 | ||||||
| chrX:38105795
|
T | A | 7 | a0001c0001t0001g0101a0001c0001t0001g0120a0001c0001t0001g0128others(4): Show | 7 | HG00544.hp1 HG02056.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1156-798T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105795 | ||||||
| chrX:38105855
|
G | A | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1156-738G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38105855 | ||||||
| chrX:38106034
|
G | A | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1156-559G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38106034 | ||||||
| chrX:38106054
|
G | A | 1 | a0001c0004t0004g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1156-539G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38106054 | ||||||
| chrX:38106178
|
C | T | 81 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1156-415C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38106178 | ||||||
| chrX:38106179
|
C | G | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1156-414C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38106179 | ||||||
| chrX:38106579
|
CT | C | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1156-12delT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | INFO_REALIGN_3_PRIME | chrX | 38106579 | |||||
| chrX:38106914
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1334+143C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38106914 | ||||||
| chrX:38107166
|
A | G | 1 | a0001c0001t0003g0193 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1334+395A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38107166 | ||||||
| chrX:38107448
|
T | C | 8 | a0002c0003t0004g0002a0002c0003t0004g0087a0002c0003t0004g0088others(5): Show | 9 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.1334+677T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38107448 | ||||||
| chrX:38107460
|
G | T | 81 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(78): Show | 82 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(79): Show |
intron_variant | MODIFIER | c.1334+689G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38107460 | ||||||
| chrX:38108185
|
C | T | 53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1335-415C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38108185 | ||||||
| chrX:38108224
|
G | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1335-376G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 11/16 | chrX | 38108224 | ||||||
| chrX:38108867
|
T | TGA | 1 | a0001c0002t0002g0066 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1434+171_1434+172d others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chrX | 38108867 | |||||
| chrX:38108887
|
T | TA | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1434+189dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chrX | 38108887 | |||||
| chrX:38108983
|
G | A | 1 | a0005c0007t0006g0065 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1434+284G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38108983 | ||||||
| chrX:38108998
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1434+299C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38108998 | ||||||
| chrX:38109089
|
T | C | 4 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1434+390T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109089 | ||||||
| chrX:38109154
|
G | A | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1434+455G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109154 | ||||||
| chrX:38109369
|
T | C | 4 | a0001c0004t0004g0233a0001c0004t0004g0234a0001c0004t0017g0231others(1): Show | 4 | HG01891.hp2 HG02451.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1434+670T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109369 | ||||||
| chrX:38109402
|
G | C | 1 | a0001c0001t0003g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1434+703G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109402 | ||||||
| chrX:38109752
|
C | T | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1435-569C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109752 | ||||||
| chrX:38109761
|
ATGT | A | 1 | a0001c0002t0002g0219 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1435-555_1435-553d others(5): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | INFO_REALIGN_3_PRIME | chrX | 38109761 | |||||
| chrX:38109770
|
C | G | 27 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(24): Show | 28 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(25): Show |
intron_variant | MODIFIER | c.1435-551C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109770 | ||||||
| chrX:38109816
|
A | G | 1 | a0001c0002t0002g0051 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1435-505A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109816 | ||||||
| chrX:38109822
|
C | T | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1435-499C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109822 | ||||||
| chrX:38109843
|
G | A | 2 | a0001c0004t0003g0230a0001c0004t0006g0171 | 2 | HG02572.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1435-478G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109843 | ||||||
| chrX:38109916
|
T | C | 1 | a0002c0003t0018g0208 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1435-405T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109916 | ||||||
| chrX:38109956
|
A | G | 1 | a0001c0001t0001g0101 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1435-365A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109956 | ||||||
| chrX:38110099
|
T | C | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1435-222T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38110099 | ||||||
| chrX:38110312
|
C | T | 3 | a0001c0002t0002g0035a0001c0002t0002g0036a0001c0002t0002g0037 | 3 | HG00544.hp2 HG00558.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.1435-9C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38110312 | ||||||
| chrX:38110650
|
G | A | 1 | a0001c0004t0002g0004 | 2 | HG03195.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1596+168G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38110650 | ||||||
| chrX:38110724
|
T | G | 4 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01934.hp1 others(1): Show |
intron_variant | MODIFIER | c.1596+242T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38110724 | ||||||
| chrX:38110804
|
C | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0132 | 2 | NA18957.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.1596+322C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38110804 | ||||||
| chrX:38111097
|
C | T | 1 | a0001c0001t0001g0074 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1596+615C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38111097 | ||||||
| chrX:38111279
|
A | C | 7 | a0001c0004t0002g0004a0001c0004t0004g0092a0001c0004t0004g0232others(4): Show | 8 | HG01891.hp2 HG02451.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.1596+797A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38111279 | ||||||
| chrX:38111375
|
G | A | 1 | a0001c0004t0002g0016 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1596+893G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38111375 | ||||||
| chrX:38111652
|
C | G | 1 | a0001c0001t0003g0229 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1596+1170C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38111652 | ||||||
| chrX:38111989
|
C | CCACAGTA others(2): Show |
53 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 53 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.1596+1511_1596+151 others(13): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38111989 | |||||
| chrX:38112156
|
T | G | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1596+1674T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112156 | ||||||
| chrX:38112276
|
G | A | 1 | a0001c0001t0008g0098 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1596+1794G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112276 | ||||||
| chrX:38112282
|
A | G | 1 | a0002c0003t0004g0158 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1596+1800A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112282 | ||||||
| chrX:38112780
|
C | T | 1 | a0003c0005t0003g0238 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.1596+2298C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112780 | ||||||
| chrX:38112837
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1596+2355C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112837 | ||||||
| chrX:38112868
|
A | T | 3 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240 | 3 | HG02723.hp2 HG03209.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1596+2386A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112868 | ||||||
| chrX:38112888
|
A | G | 1 | a0001c0001t0012g0154 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1596+2406A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38112888 | ||||||
| chrX:38113159
|
C | T | 1 | a0001c0004t0002g0242 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1596+2677C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113159 | ||||||
| chrX:38113300
|
TC | T | 1 | a0002c0003t0004g0164 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1596+2819delC | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113300 | ||||||
| chrX:38113421
|
T | A | 1 | a0001c0001t0003g0200 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1596+2939T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113421 | ||||||
| chrX:38113480
|
G | A | 24 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055others(21): Show | 25 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.1596+2998G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113480 | ||||||
| chrX:38113607
|
T | C | 88 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0012others(85): Show | 90 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(87): Show |
intron_variant | MODIFIER | c.1596+3125T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113607 | ||||||
| chrX:38113898
|
G | A | 1 | a0001c0001t0014g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1596+3416G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113898 | ||||||
| chrX:38114222
|
C | T | 1 | a0001c0001t0003g0174 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1596+3740C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38114222 | ||||||
| chrX:38114526
|
A | G | 89 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0002t0002g0010others(86): Show | 92 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(89): Show |
intron_variant | MODIFIER | c.1596+4044A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38114526 | ||||||
| chrX:38115098
|
C | A | 1 | a0001c0001t0001g0111 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1596+4616C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115098 | ||||||
| chrX:38115136
|
T | G | 18 | a0001c0001t0003g0005a0001c0001t0003g0102a0001c0001t0003g0106others(15): Show | 18 | HG00099.hp1 HG00741.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.1596+4654T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115136 | ||||||
| chrX:38115179
|
G | A | 1 | a0004c0006t0001g0137 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1596+4697G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115179 | ||||||
| chrX:38115187
|
TAAGATAC others(314): Show |
T | 8 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(5): Show | 8 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(5): Show |
intron_variant | MODIFIER | c.1596+4721_1597-483 others(4): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115187 | |||||
| chrX:38115250
|
C | T | 1 | a0001c0002t0002g0062 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1596+4768C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115250 | ||||||
| chrX:38115328
|
C | T | 7 | a0001c0004t0002g0016a0001c0004t0002g0026a0001c0004t0002g0068others(4): Show | 7 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.1596+4846C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115328 | ||||||
| chrX:38115353
|
G | A | 2 | a0001c0001t0003g0223a0001c0001t0014g0177 | 2 | HG02683.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.1596+4871G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115353 | ||||||
| chrX:38115483
|
C | CA | 50 | a0001c0001t0001g0072a0001c0001t0001g0074a0001c0001t0001g0095others(47): Show | 51 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(48): Show |
intron_variant | MODIFIER | c.1597-4848dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115483 | |||||
| chrX:38115483
|
C | CAA | 4 | a0001c0001t0001g0151a0001c0002t0002g0070a0001c0002t0002g0245others(1): Show | 4 | HG01934.hp1 HG02055.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1597-4849_1597-484 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115483 | |||||
| chrX:38115483
|
C | CAAA | 1 | a0002c0003t0004g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1597-4850_1597-484 others(7): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115483 | |||||
| chrX:38115483
|
C | CAAAAA | 1 | a0001c0004t0002g0068 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1597-4852_1597-484 others(9): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115483 | |||||
| chrX:38115483
|
CA | C | 11 | a0001c0001t0001g0124a0001c0001t0001g0133a0001c0001t0001g0166others(8): Show | 11 | HG00639.hp1 HG01255.hp1 HG02572.hp1 others(8): Show |
intron_variant | MODIFIER | c.1597-4848delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115483 | |||||
| chrX:38115585
|
CACTT | C | 1 | a0003c0005t0004g0235 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1597-4769_1597-476 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38115585 | |||||
| chrX:38115709
|
G | A | 1 | a0001c0002t0002g0241 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1597-4649G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115709 | ||||||
| chrX:38115763
|
T | A | 1 | a0001c0001t0003g0212 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1597-4595T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115763 | ||||||
| chrX:38115908
|
G | A | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1597-4450G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38115908 | ||||||
| chrX:38116307
|
AG | A | 4 | a0001c0002t0002g0010a0001c0002t0002g0011a0001c0002t0002g0058others(1): Show | 4 | HG02145.hp1 HG02258.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-4050delG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116307 | ||||||
| chrX:38116311
|
C | T | 5 | a0001c0002t0002g0039a0001c0002t0002g0040a0001c0002t0002g0042others(2): Show | 5 | HG00639.hp2 HG01109.hp1 HG02004.hp2 others(2): Show |
intron_variant | MODIFIER | c.1597-4047C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116311 | ||||||
| chrX:38116468
|
C | A | 1 | a0001c0001t0003g0159 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1597-3890C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116468 | ||||||
| chrX:38116532
|
T | C | 5 | a0001c0001t0003g0209a0001c0001t0003g0210a0001c0001t0003g0214others(2): Show | 5 | HG02071.hp1 NA18945.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-3826T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116532 | ||||||
| chrX:38116618
|
T | C | 2 | a0001c0004t0017g0231a0001c0004t0022g0030 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1597-3740T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116618 | ||||||
| chrX:38116792
|
T | C | 81 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(78): Show | 84 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(81): Show |
intron_variant | MODIFIER | c.1597-3566T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116792 | ||||||
| chrX:38116845
|
T | C | 1 | a0002c0003t0006g0024 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1597-3513T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38116845 | ||||||
| chrX:38117324
|
G | A | 6 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-3034G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117324 | ||||||
| chrX:38117325
|
G | T | 6 | a0001c0002t0002g0027a0001c0002t0002g0237a0001c0002t0002g0240others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-3033G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117325 | ||||||
| chrX:38117366
|
G | A | 8 | a0001c0004t0002g0016a0001c0004t0002g0026a0001c0004t0002g0068others(5): Show | 8 | HG01891.hp1 HG02280.hp1 HG02559.hp1 others(5): Show |
intron_variant | MODIFIER | c.1597-2992G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117366 | ||||||
| chrX:38117441
|
C | G | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1597-2917C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117441 | ||||||
| chrX:38117455
|
C | T | 1 | a0001c0001t0001g0173 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1597-2903C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117455 | ||||||
| chrX:38117540
|
C | A | 1 | a0001c0001t0001g0162 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1597-2818C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117540 | ||||||
| chrX:38117614
|
C | T | 1 | a0002c0003t0004g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1597-2744C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117614 | ||||||
| chrX:38117961
|
C | A | 7 | a0001c0001t0004g0168a0003c0005t0002g0001a0003c0005t0002g0006others(4): Show | 8 | HG01261.hp1 HG01496.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.1597-2397C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38117961 | ||||||
| chrX:38118071
|
T | G | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1597-2287T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118071 | ||||||
| chrX:38118160
|
T | C | 1 | a0001c0001t0003g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1597-2198T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118160 | ||||||
| chrX:38118417
|
C | T | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1597-1941C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118417 | ||||||
| chrX:38118418
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0126a0001c0001t0001g0135others(1): Show | 4 | HG02074.hp1 NA18946.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.1597-1940G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118418 | ||||||
| chrX:38118609
|
C | T | 2 | a0001c0001t0001g0122a0001c0001t0001g0140 | 2 | NA19009.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.1597-1749C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118609 | ||||||
| chrX:38118825
|
G | C | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1597-1533G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118825 | ||||||
| chrX:38118920
|
A | AATATATA others(3): Show |
1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1597-1427_1597-141 others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(13): Show |
1 | a0001c0004t0002g0007 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1597-1437_1597-141 others(24): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(15): Show |
3 | a0001c0002t0002g0240a0001c0002t0002g0244a0001c0004t0002g0008 | 3 | HG02622.hp2 HG03486.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1597-1418_1597-141 others(26): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(17): Show |
1 | a0001c0002t0002g0237 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1597-1418_1597-141 others(28): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(23): Show |
1 | a0001c0004t0002g0049 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1597-1418_1597-141 others(34): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(23): Show |
1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1597-1420_1597-141 others(34): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
A | AATATATA others(21): Show |
2 | a0001c0004t0010g0017a0001c0004t0010g0018 | 2 | HG02559.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.1597-1422_1597-142 others(32): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
AAT | A | 132 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.1597-1419_1597-141 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118920
|
AATAT | A | 81 | a0001c0001t0003g0129a0001c0001t0003g0223a0001c0001t0004g0003others(78): Show | 85 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(82): Show |
intron_variant | MODIFIER | c.1597-1421_1597-141 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118920 | |||||
| chrX:38118924
|
T | TATATATA others(57): Show |
1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1597-1418_1597-141 others(68): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118924 | |||||
| chrX:38118937
|
A | G | 20 | a0001c0001t0004g0168a0001c0001t0004g0195a0001c0002t0002g0013others(17): Show | 20 | HG00544.hp2 HG00558.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1597-1421A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118937 | ||||||
| chrX:38118938
|
T | TACGC | 6 | a0001c0001t0004g0168a0001c0002t0002g0013a0001c0002t0002g0014others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-1419_1597-141 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118938 | |||||
| chrX:38118940
|
T | C | 14 | a0001c0001t0004g0195a0001c0002t0002g0035a0001c0002t0002g0036others(11): Show | 14 | HG00544.hp2 HG00558.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1597-1418T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118940 | ||||||
| chrX:38118941
|
G | A | 6 | a0001c0001t0004g0168a0001c0002t0002g0013a0001c0002t0002g0014others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-1417G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118941 | ||||||
| chrX:38118941
|
G | GCA | 14 | a0001c0001t0004g0195a0001c0002t0002g0035a0001c0002t0002g0036others(11): Show | 14 | HG00544.hp2 HG00558.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1597-1417_1597-141 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118941 | ||||||
| chrX:38118944
|
C | T | 14 | a0001c0001t0004g0195a0001c0002t0002g0035a0001c0002t0002g0036others(11): Show | 14 | HG00544.hp2 HG00558.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1597-1414C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118944 | ||||||
| chrX:38118945
|
G | A | 20 | a0001c0001t0004g0168a0001c0001t0004g0195a0001c0002t0002g0013others(17): Show | 20 | HG00544.hp2 HG00558.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1597-1413G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118945 | ||||||
| chrX:38118946
|
C | T | 6 | a0001c0001t0004g0168a0001c0002t0002g0013a0001c0002t0002g0014others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.1597-1412C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118946 | ||||||
| chrX:38118952
|
C | CAT | 10 | a0001c0001t0001g0075a0001c0001t0001g0172a0001c0001t0001g0173others(7): Show | 10 | HG00733.hp2 HG01106.hp1 HG02083.hp1 others(7): Show |
intron_variant | MODIFIER | c.1597-1387_1597-138 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118952 | |||||
| chrX:38118952
|
C | CATAT | 53 | a0001c0001t0004g0003a0001c0002t0002g0011a0001c0002t0002g0012others(50): Show | 56 | HG00597.hp1 HG00639.hp2 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.1597-1389_1597-138 others(8): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118952 | |||||
| chrX:38118952
|
C | CATATATA others(3): Show |
1 | a0001c0002t0002g0010 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1597-1395_1597-138 others(14): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118952 | |||||
| chrX:38118952
|
C | T | 20 | a0001c0001t0004g0168a0001c0001t0004g0195a0001c0002t0002g0013others(17): Show | 20 | HG00544.hp2 HG00558.hp1 HG01884.hp2 others(17): Show |
intron_variant | MODIFIER | c.1597-1406C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118952 | ||||||
| chrX:38118952
|
CAT | C | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1597-1387_1597-138 others(6): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118952 | |||||
| chrX:38118954
|
T | TATATATA others(23): Show |
1 | a0001c0001t0006g0033 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1597-1395_1597-136 others(34): Show |
SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | INFO_REALIGN_3_PRIME | chrX | 38118954 | |||||
| chrX:38118976
|
C | T | 1 | a0001c0002t0002g0244 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1597-1382C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38118976 | ||||||
| chrX:38119117
|
A | G | 1 | a0001c0001t0005g0054 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.1597-1241A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38119117 | ||||||
| chrX:38119175
|
C | T | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1597-1183C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38119175 | ||||||
| chrX:38119237
|
C | A | 5 | a0001c0002t0002g0237a0001c0002t0002g0240a0001c0004t0002g0007others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1597-1121C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38119237 | ||||||
| chrX:38119374
|
T | C | 1 | a0001c0002t0004g0091 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1597-984T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38119374 | ||||||
| chrX:38119393
|
A | C | 1 | a0001c0001t0003g0184 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1597-965A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38119393 | ||||||
| chrX:38120203
|
C | A | 98 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(95): Show | 102 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.1597-155C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38120203 | ||||||
| chrX:38120219
|
C | T | 1 | a0001c0002t0002g0057 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1597-139C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38120219 | ||||||
| chrX:38120514
|
A | C | 72 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(69): Show | 75 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(72): Show |
intron_variant | MODIFIER | c.1705+48A>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38120514 | ||||||
| chrX:38120601
|
T | G | 2 | a0001c0001t0001g0147a0001c0002t0002g0143 | 2 | HG02602.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.1705+135T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38120601 | ||||||
| chrX:38120688
|
C | A | 1 | a0001c0002t0002g0217 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1705+222C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38120688 | ||||||
| chrX:38120805
|
T | C | 2 | a0001c0001t0001g0112a0001c0001t0001g0141 | 2 | HG00597.hp2 HG00673.hp1 |
intron_variant | MODIFIER | c.1705+339T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38120805 | ||||||
| chrX:38121044
|
G | A | 1 | a0001c0001t0003g0189 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1705+578G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121044 | ||||||
| chrX:38121073
|
G | A | 4 | a0001c0002t0002g0027a0001c0004t0002g0016a0001c0004t0002g0068others(1): Show | 4 | HG01891.hp1 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1705+607G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121073 | ||||||
| chrX:38121309
|
C | T | 1 | a0001c0001t0014g0177 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1706-771C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121309 | ||||||
| chrX:38121352
|
C | G | 6 | a0001c0002t0002g0237a0001c0002t0002g0240a0001c0002t0002g0244others(3): Show | 6 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.1706-728C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121352 | ||||||
| chrX:38121381
|
C | CT | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1706-695dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chrX | 38121381 | |||||
| chrX:38121602
|
C | T | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1706-478C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121602 | ||||||
| chrX:38121666
|
T | TA | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1706-410dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chrX | 38121666 | |||||
| chrX:38121678
|
G | T | 7 | a0001c0004t0002g0004a0001c0004t0017g0231a0001c0004t0022g0030others(4): Show | 8 | HG01255.hp1 HG01884.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1706-402G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121678 | ||||||
| chrX:38121693
|
T | G | 1 | a0001c0002t0002g0143 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1706-387T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121693 | ||||||
| chrX:38121780
|
AG | A | 3 | a0001c0002t0002g0070a0001c0002t0002g0071a0001c0002t0002g0245 | 3 | HG02055.hp1 HG02280.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1706-298delG | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chrX | 38121780 | |||||
| chrX:38121874
|
C | A | 1 | a0001c0002t0004g0176 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1706-206C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121874 | ||||||
| chrX:38121911
|
C | CA | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1706-164dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chrX | 38121911 | |||||
| chrX:38121918
|
G | GT | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1706-159dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | INFO_REALIGN_3_PRIME | chrX | 38121918 | |||||
| chrX:38122021
|
G | A | 1 | a0002c0003t0004g0089 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1706-59G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38122021 | ||||||
| chrX:38122221
|
T | A | 98 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(95): Show | 102 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(99): Show |
splice_region_variant&intron_variant | LOW | c.1841+6T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122221 | ||||||
| chrX:38122263
|
A | G | 3 | a0001c0004t0002g0007a0001c0004t0002g0008a0001c0004t0002g0049 | 3 | HG02622.hp2 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1841+48A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122263 | ||||||
| chrX:38122443
|
C | G | 2 | a0001c0001t0001g0128a0001c0001t0001g0139 | 2 | HG00544.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.1841+228C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122443 | ||||||
| chrX:38122490
|
G | A | 2 | a0001c0004t0017g0231a0001c0004t0022g0030 | 2 | HG01891.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1841+275G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122490 | ||||||
| chrX:38122692
|
A | G | 7 | a0001c0002t0002g0237a0001c0002t0002g0240a0001c0002t0002g0244others(4): Show | 7 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.1841+477A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122692 | ||||||
| chrX:38122727
|
C | CA | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1841+515dupA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chrX | 38122727 | |||||
| chrX:38122805
|
C | T | 5 | a0001c0002t0002g0237a0001c0002t0002g0240a0001c0004t0002g0007others(2): Show | 5 | HG02622.hp2 HG02723.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.1841+590C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122805 | ||||||
| chrX:38122948
|
T | C | 3 | a0001c0001t0008g0097a0001c0001t0008g0098a0001c0001t0019g0041 | 3 | HG01952.hp1 HG01993.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.1841+733T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122948 | ||||||
| chrX:38122971
|
C | T | 2 | a0001c0001t0001g0156a0001c0001t0001g0166 | 2 | HG00639.hp1 HG01069.hp1 |
intron_variant | MODIFIER | c.1841+756C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38122971 | ||||||
| chrX:38123135
|
T | C | 1 | a0001c0002t0002g0059 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1841+920T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123135 | ||||||
| chrX:38123336
|
C | T | 1 | a0001c0001t0003g0005 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1841+1121C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123336 | ||||||
| chrX:38123368
|
A | T | 1 | a0001c0008t0004g0160 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1841+1153A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123368 | ||||||
| chrX:38123502
|
G | T | 1 | a0001c0001t0002g0009 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1841+1287G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123502 | ||||||
| chrX:38123635
|
G | T | 1 | a0003c0005t0002g0056 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1841+1420G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123635 | ||||||
| chrX:38123979
|
G | GT | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1842-1311dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chrX | 38123979 | |||||
| chrX:38124042
|
G | A | 1 | a0001c0001t0001g0100 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1842-1256G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124042 | ||||||
| chrX:38124362
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1842-936G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124362 | ||||||
| chrX:38124515
|
A | AT | 1 | a0008c0013t0009g0116 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1842-778dupT | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | INFO_REALIGN_3_PRIME | chrX | 38124515 | |||||
| chrX:38124553
|
A | T | 90 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(87): Show | 94 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1842-745A>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124553 | ||||||
| chrX:38124667
|
A | G | 3 | a0002c0003t0002g0044a0002c0003t0002g0046a0002c0003t0002g0055 | 3 | HG01884.hp1 HG03098.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1842-631A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124667 | ||||||
| chrX:38124815
|
C | T | 1 | a0001c0004t0002g0236 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1842-483C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124815 | ||||||
| chrX:38124881
|
G | A | 90 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(87): Show | 94 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.1842-417G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124881 | ||||||
| chrX:38124914
|
T | G | 1 | a0001c0004t0004g0232 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1842-384T>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124914 | ||||||
| chrX:38124981
|
G | A | 1 | a0002c0003t0004g0090 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1842-317G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124981 | ||||||
| chrX:38125067
|
A | G | 91 | a0001c0001t0004g0003a0001c0001t0004g0168a0001c0001t0004g0195others(88): Show | 95 | HG00544.hp2 HG00558.hp1 HG00597.hp1 others(92): Show |
intron_variant | MODIFIER | c.1842-231A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38125067 | ||||||
| chrX:38126573
|
G | A | 5 | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0001g0121others(2): Show | 5 | NA18966.hp1 NA18984.hp1 NA18990.hp1 others(2): Show |
intron_variant | MODIFIER | c.2051-15G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 16/16 | chrX | 38126573 |