Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 730 | 213 | 53 | 33 | 93 | 7 | 25 | 66 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| a0002 | 0/0 | 730 | 25 | 10 | 9 | 1 | 0 | 5 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| a0003 | 0/0 | 730 | 9 | 5 | 2 | 0 | 0 | 2 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| a0004 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| a0005 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| a0006 | 0/0 | 730 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | MSKNS others(725): Show |
chrX | 38001553 | 38133816 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2190 | 138 | 5 | 24 | 80 | 7 | 20 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0001c0002 | 0/0 | 2190 | 52 | 26 | 9 | 12 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0001c0004 | 0/0 | 2190 | 21 | 21 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0001c0008 | 0/0 | 2190 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0001c0010 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0002c0003 | 0/0 | 2190 | 25 | 10 | 9 | 1 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0003c0005 | 0/0 | 2190 | 8 | 5 | 2 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0003c0007 | 0/0 | 2190 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0004c0006 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0005c0011 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 | ||
| a0006c0009 | 0/0 | 2190 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | ATGTC others(2185): Show |
chrX | 38001553 | 38133816 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 4751 | 76 | 2 | 18 | 43 | 5 | 6 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0002 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0003 | 0/0 | 4751 | 41 | 0 | 3 | 26 | 2 | 10 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0004 | 0/0 | 4751 | 5 | 1 | 0 | 1 | 0 | 3 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0005 | 0/0 | 4751 | 6 | 0 | 0 | 6 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0006 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0008 | 0/0 | 4751 | 2 | 0 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0012 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0013 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0014 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0015 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0016 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0001t0019 | 0/0 | 4751 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0002 | 0/0 | 4751 | 42 | 24 | 8 | 6 | 0 | 4 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0004 | 0/0 | 4751 | 4 | 1 | 1 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0009 | 0/0 | 4751 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0011 | 0/0 | 4751 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0020 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0002t0021 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0002 | 0/0 | 4751 | 10 | 10 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0003 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0004 | 0/0 | 4751 | 4 | 4 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0006 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0010 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0017 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0022 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0004t0023 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0008t0004 | 0/0 | 4751 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0001c0010t0005 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0002c0003t0002 | 0/0 | 4751 | 5 | 5 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0002c0003t0004 | 0/0 | 4751 | 14 | 0 | 8 | 1 | 0 | 5 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0002c0003t0006 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0002c0003t0007 | 0/0 | 4751 | 3 | 3 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0002c0003t0018 | 0/0 | 4751 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0003c0005t0002 | 0/0 | 4751 | 5 | 3 | 2 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0003c0005t0003 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0003c0005t0004 | 0/0 | 4751 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0003c0007t0006 | 0/0 | 4751 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0004c0006t0001 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0005c0011t0003 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| a0006c0009t0001 | 0/0 | 4751 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | GGTTT others(4746): Show |
chrX | 38001553 | 38133816 |
| actghapid | grch38/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 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0102 | 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 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0107 | 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 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 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 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 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 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0127 | 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 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 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 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 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 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0159 | 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 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0002g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0009 | 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 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0179 | 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 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0205 | 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 |
| a0001c0001t0003g0208 | 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 |
| a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0004g0005 | 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 |
| a0001c0001t0004g0188 | 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 |
| a0001c0001t0005g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0005g0065 | 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 |
| a0001c0001t0006g0037 | 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 |
| a0001c0001t0012g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0013g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0001t0014g0175 | 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 |
| a0001c0001t0019g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0002 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0007 | 0/0 | 2 | 0 | 2 | 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 |
| a0001c0002t0002g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 | 0 | 1 | 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 |
| a0001c0002t0002g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0002t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 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 |
| 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 |
| 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 |
| a0001c0002t0004g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0004g0178 | 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 |
| a0001c0002t0009g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0011g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0002t0011g0054 | 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 |
| a0001c0002t0021g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0030 | 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 |
| a0001c0004t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0003g0233 | 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 |
| a0001c0004t0004g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0004g0229 | 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 |
| a0001c0004t0010g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0017g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0022g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0004t0023g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0008t0004g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0001c0010t0005g0035 | 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 |
| a0002c0003t0002g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0004g0004 | 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 |
| a0002c0003t0004g0160 | 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 |
| a0002c0003t0004g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0006g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0006g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0002c0003t0018g0206 | 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 |
| a0003c0005t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0005t0003g0234 | 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 |
| a0003c0005t0004g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0003c0007t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0004c0006t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| a0005c0011t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0003 | g0104 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0223 | EUR | GBR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0117 | EUR | FIN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00544 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00544 | hp2 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00558 | hp1 | a0001 | c0002 | t0002 | g0038 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00597 | hp1 | a0001 | c0002 | t0004 | g0178 | EAS | CHS | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0114 | 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 | g0043 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00642 | hp1 | a0002 | c0003 | t0004 | g0199 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0143 | 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 | g0099 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0222 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00741 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG00741 | hp2 | a0001 | c0001 | t0003 | g0131 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0112 | 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 | g0129 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01167 | hp1 | a0002 | c0003 | t0004 | g0004 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01168 | hp2 | a0002 | c0003 | t0018 | g0206 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01169 | hp1 | a0002 | c0003 | t0004 | g0004 | AMR | PUR | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0150 | 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 | g0007 | 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 | g0007 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0120 | 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 | g0214 | 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 | g0110 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0212 | 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 | g0200 | AMR | CLM | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0147 | 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 | g0019 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01891 | hp1 | a0001 | c0004 | t0002 | g0020 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01891 | hp2 | a0001 | c0004 | t0022 | g0034 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01928 | hp1 | a0001 | c0002 | t0002 | g0215 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0140 | 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 | g0042 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG01993 | hp2 | a0001 | c0002 | t0002 | g0217 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02004 | hp2 | a0001 | c0002 | t0002 | g0041 | AMR | PEL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02015 | hp1 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02055 | hp1 | a0001 | c0002 | t0002 | g0241 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02071 | hp1 | a0001 | c0001 | t0003 | g0210 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02080 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0180 | 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 | g0100 | 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 | g0015 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02148 | hp1 | a0001 | c0002 | t0002 | g0040 | 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 | g0204 | EAS | CDX | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | CDX | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02258 | hp1 | a0001 | c0002 | t0002 | g0235 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02280 | hp1 | a0001 | c0004 | t0002 | g0070 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02280 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02451 | hp1 | a0001 | c0004 | t0004 | g0229 | 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 | g0039 | 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 | g0149 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02622 | hp1 | a0001 | c0002 | t0002 | g0237 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02622 | hp2 | a0001 | c0004 | t0002 | g0012 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02630 | hp1 | a0002 | c0003 | t0006 | g0029 | 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 | g0060 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02683 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02683 | hp2 | a0001 | c0002 | t0002 | g0052 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02698 | hp1 | a0003 | c0007 | t0006 | g0068 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02717 | hp1 | a0003 | c0005 | t0002 | g0032 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02723 | hp1 | a0001 | c0004 | t0002 | g0238 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02723 | hp2 | a0001 | c0002 | t0002 | g0232 | 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 | g0151 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0014 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02809 | hp2 | a0002 | c0003 | t0007 | g0026 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02886 | hp1 | a0003 | c0005 | t0002 | g0010 | 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 | g0018 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02922 | hp1 | a0001 | c0002 | t0002 | g0071 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02922 | hp2 | a0002 | c0003 | t0007 | g0025 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02965 | hp1 | a0001 | c0002 | t0002 | g0053 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02970 | hp1 | a0002 | c0003 | t0006 | g0028 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02970 | hp2 | a0001 | c0002 | t0002 | g0062 | 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 | g0033 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03041 | hp2 | a0001 | c0001 | t0006 | g0037 | 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 | g0013 | 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 | g0008 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03195 | hp2 | a0003 | c0005 | t0004 | g0230 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03209 | hp1 | a0001 | c0002 | t0002 | g0031 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03225 | hp1 | a0001 | c0002 | t0002 | g0016 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03453 | hp1 | a0001 | c0002 | t0021 | g0024 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03453 | hp2 | a0001 | c0004 | t0002 | g0030 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03486 | hp1 | a0001 | c0004 | t0002 | g0231 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03486 | hp2 | a0001 | c0002 | t0002 | g0236 | 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 | g0234 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03491 | hp2 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03492 | hp1 | a0001 | c0001 | t0004 | g0005 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03516 | hp1 | a0001 | c0004 | t0002 | g0011 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03516 | hp2 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03540 | hp1 | a0001 | c0004 | t0003 | g0233 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03540 | hp2 | a0001 | c0004 | t0017 | g0226 | AFR | GWD | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03579 | hp1 | a0002 | c0003 | t0002 | g0057 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03654 | hp1 | a0001 | c0001 | t0003 | g0157 | 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 | g0108 | 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 | g0211 | 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 | g0126 | SAS | PJL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03831 | hp1 | a0001 | c0001 | t0014 | g0175 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03831 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03834 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03834 | hp2 | a0001 | c0001 | t0004 | g0188 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03927 | hp2 | a0001 | c0002 | t0002 | g0050 | SAS | BEB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03942 | hp1 | a0001 | c0002 | t0002 | g0145 | 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 | g0201 | 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 | g0221 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04204 | hp1 | a0001 | c0001 | t0003 | g0146 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG04228 | hp1 | a0001 | c0001 | t0003 | g0009 | SAS | STU | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18522 | hp1 | a0001 | c0008 | t0004 | g0101 | 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 | g0103 | EAS | CHB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18906 | hp1 | a0002 | c0003 | t0002 | g0239 | 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 | g0006 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18939 | hp2 | a0004 | c0006 | t0001 | g0139 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18940 | hp1 | a0001 | c0002 | t0011 | g0054 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18943 | hp1 | a0001 | c0001 | t0003 | g0198 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18944 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18945 | hp1 | a0001 | c0001 | t0003 | g0207 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18946 | hp2 | a0001 | c0001 | t0003 | g0176 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18948 | hp1 | a0001 | c0002 | t0002 | g0216 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18950 | hp2 | a0001 | c0002 | t0011 | g0036 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18952 | hp1 | a0001 | c0001 | t0005 | g0056 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18953 | hp1 | a0001 | c0001 | t0003 | g0185 | 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 | g0132 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18957 | hp1 | a0001 | c0002 | t0002 | g0069 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18959 | hp1 | a0001 | c0001 | t0005 | g0051 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18961 | hp1 | a0001 | c0001 | t0003 | g0182 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18964 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18964 | hp2 | a0001 | c0001 | t0005 | g0065 | 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 | g0116 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18967 | hp1 | a0001 | c0002 | t0009 | g0118 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18970 | hp1 | a0001 | c0001 | t0003 | g0155 | 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 | a0005 | c0011 | t0003 | g0190 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18982 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18983 | hp1 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0186 | 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 | g0122 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0135 | 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 | g0184 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19000 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19002 | hp1 | a0001 | c0001 | t0013 | g0203 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19002 | hp2 | a0001 | c0001 | t0012 | g0156 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19004 | hp1 | a0001 | c0001 | t0005 | g0055 | 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 | g0205 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19012 | hp1 | a0001 | c0002 | t0002 | g0059 | 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 | g0061 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19043 | hp1 | a0001 | c0004 | t0023 | g0023 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19055 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19056 | hp1 | a0001 | c0001 | t0003 | g0006 | 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 | g0121 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19062 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0144 | 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 | g0105 | 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 | g0115 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0123 | 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 | g0136 | EAS | JPT | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19082 | hp1 | a0001 | c0001 | t0003 | g0213 | 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 | g0160 | 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 | g0035 | 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 | g0058 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA19240 | hp2 | a0001 | c0002 | t0002 | g0240 | AFR | YRI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20129 | hp1 | a0001 | c0004 | t0004 | g0228 | AFR | ASW | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20129 | hp2 | a0001 | c0002 | t0002 | g0063 | 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 | g0187 | EUR | TSI | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0109 | SAS | GIH | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02109 | hp1 | a0001 | c0002 | t0002 | g0064 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02109 | hp2 | a0001 | c0002 | t0002 | g0017 | 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 | g0021 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG02559 | hp2 | a0002 | c0003 | t0007 | g0027 | AFR | ACB | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG03471 | hp1 | a0001 | c0004 | t0010 | g0022 | AFR | MSL | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG06807 | hp1 | a0001 | c0004 | t0004 | g0227 | AFR | USA | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| HG06807 | hp2 | a0001 | c0004 | t0002 | g0008 | 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 | g0209 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| NA21309 | hp2 | a0002 | c0003 | t0002 | g0066 | AFR | LWK | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0095 | REF | REF | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0163 | REF | REF | SYTL5_chrX_38001553_38133816 | SYTL5 | chrX | 38001553 | 38133816 |
| view | 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 | a0005 | 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 | a0003 | 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 |
| view | 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 | 3 | a0001c0002 a0002c0003 a0003c0005 |
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 | 5 | a0001c0002 a0001c0004 a0001c0008 others(2): 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 |
| view | 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 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0006 others(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 | 20 | a0001c0001t0002 a0001c0001t0004 a0001c0002t0002 others(17): 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 | 33 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(30): 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 | 2 | a0001c0002t0009 a0001c0002t0011 |
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 | a0001c0004t0017 a0001c0004t0022 |
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 | a0001c0001t0008 a0001c0001t0019 |
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 |
| view | 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 | a0001c0001t0003g0009 | 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 76 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(73): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0021g0024 others(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 | a0003c0005t0002g0010 | 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0003g0242 | 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 | a0001c0004t0002g0020 a0001c0004t0010g0021 a0001c0004t0010g0022 |
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 | a0001c0004t0022g0034 | 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 | 76 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(73): 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 | 76 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(73): 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 | 76 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(73): 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 | 59 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(56): 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:38008893 | T | C | 1 | a0001c0004t0023g0023 | 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:38009717 | A | G | 1 | a0001c0001t0003g0225 | 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 | a0001c0001t0003g0224 | 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 | 40 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(37): 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 | 76 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(73): 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0003c0005t0002g0032 |
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 | 40 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(37): 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 | a0001c0004t0002g0030 | 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 | a0001c0004t0002g0011 a0001c0004t0002g0012 |
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 | a0001c0001t0001g0222 a0001c0001t0001g0223 a0001c0001t0003g0219 others(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 | 218 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(215): Show |
224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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:38011881 | A | ATT | 38 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(35): 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 | a0001c0004t0004g0227 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0001c0002t0002g0071 | 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 | a0001c0002t0021g0024 a0002c0003t0007g0025 a0002c0003t0007g0026 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0004t0002g0070 others(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 | a0001c0001t0001g0081 a0001c0001t0003g0082 |
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 | a0001c0004t0002g0020 | 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0002t0021g0024 | 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 | a0001c0002t0002g0232 a0001c0004t0002g0231 |
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 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0004t0002g0030 | 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 | 39 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(36): 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 | 157 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0001g0172 others(154): Show |
164 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(161): Show |
intron_variant | MODIFIER | c.-357+9004G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38015672 | |||||||
| chrX:38015736 | G | T | 1 | a0002c0003t0004g0160 | 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 | 15 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(12): Show |
16 | HG00733.hp1 HG01167.hp1 HG01169.hp1 others(13): 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 | a0001c0001t0001g0159 | 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 | a0001c0002t0002g0019 | 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 | a0001c0001t0006g0037 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0166 |
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:38016425 | T | C | 3 | a0001c0002t0002g0002 a0001c0002t0002g0038 a0001c0002t0002g0039 |
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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | a0001c0004t0023g0023 | 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | 39 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(36): 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0004t0002g0070 others(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 | 40 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(37): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0004t0023g0023 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0004t0002g0070 others(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 | a0001c0001t0001g0218 | 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 | a0001c0002t0002g0240 a0001c0004t0002g0008 a0002c0003t0002g0239 |
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 | 87 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(84): 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 | a0001c0001t0003g0213 | 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 | 1 | a0001c0002t0002g0003 | 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0001t0002g0013 a0001c0004t0002g0020 a0001c0004t0010g0021 others(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:38019965 | G | A | 87 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(84): 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 | a0001c0001t0019g0042 a0001c0002t0002g0040 a0001c0002t0002g0041 others(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 | a0001c0002t0002g0014 | 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 | a0003c0005t0003g0234 | 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 | a0001c0001t0003g0219 a0001c0001t0003g0242 a0001c0002t0002g0071 others(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 | CAT | C | 29 | a0001c0001t0001g0100 a0001c0001t0003g0099 a0001c0001t0003g0177 others(26): 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 | 41 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0102 others(38): 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 | 42 | a0001c0001t0001g0083 a0001c0001t0001g0107 a0001c0001t0001g0110 others(39): 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 | a0001c0001t0001g0072 a0001c0001t0001g0075 a0001c0001t0001g0076 others(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 | a0001c0001t0001g0147 a0001c0001t0001g0148 a0001c0001t0001g0149 others(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 | a0001c0001t0001g0154 a0001c0004t0010g0022 |
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 | a0001c0004t0002g0030 a0001c0004t0002g0238 a0002c0003t0006g0028 others(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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0012g0156 others(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:38020739 | A | G | 96 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(93): Show |
102 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(99): 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 | a0001c0001t0001g0144 | 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 | 8 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0038 others(5): 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 | a0001c0001t0003g0157 | 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 | 87 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(84): 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 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 |
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 | a0003c0005t0003g0234 | 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 | a0001c0001t0001g0204 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0004t0002g0070 others(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 | a0001c0001t0003g0189 a0005c0011t0003g0190 |
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 | a0001c0001t0001g0102 | 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 | a0001c0002t0002g0059 | 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 | a0001c0001t0013g0203 | 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0200 others(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 | 103 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(100): Show |
109 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(106): Show |
intron_variant | MODIFIER | c.-356-9587A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38023947 | |||||||
| chrX:38024050 | G | GA | 52 | a0001c0001t0001g0073 a0001c0001t0001g0172 a0001c0001t0001g0173 others(49): 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0003g0198 a0001c0001t0003g0242 |
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 | 80 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(77): 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 | 16 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(13): Show |
17 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(14): 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 | a0001c0002t0002g0232 a0001c0002t0002g0235 a0001c0002t0002g0236 others(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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | a0001c0001t0001g0212 | 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 | a0001c0001t0003g0009 | 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0002g0232 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | a0001c0001t0003g0146 | 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 | a0001c0004t0023g0023 | 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0004t0002g0238 | 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 | a0001c0001t0001g0149 | 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 | a0001c0002t0002g0053 a0001c0002t0002g0241 |
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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | a0001c0001t0003g0207 | 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 | a0001c0001t0001g0107 | 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 | a0001c0001t0005g0065 | 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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:38027824 | C | CT | 13 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 73 | a0001c0001t0001g0107 a0001c0001t0001g0115 a0001c0001t0001g0116 others(70): 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 | a0001c0002t0002g0214 a0001c0004t0003g0233 a0001c0004t0004g0227 others(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 | a0001c0001t0001g0148 | 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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0002t0002g0060 | 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 | 17 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(14): Show |
18 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.-356-5266T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38028268 | |||||||
| chrX:38028339 | T | C | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | a0001c0002t0002g0232 | 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 | a0003c0005t0003g0234 | 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | a0003c0005t0002g0058 | 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 107 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(104): Show |
113 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(110): 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | a0001c0001t0001g0114 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0003g0207 | 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 | 107 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(104): Show |
113 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(110): Show |
intron_variant | MODIFIER | c.-356-2966T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38030568 | |||||||
| chrX:38030658 | A | G | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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:38031259 | C | T | 1 | a0001c0002t0002g0069 | 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 | a0001c0002t0002g0232 a0001c0004t0002g0231 |
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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0001t0001g0117 a0001c0001t0001g0172 |
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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0002t0021g0024 a0001c0004t0002g0030 a0001c0004t0006g0171 others(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 | a0003c0005t0003g0234 | 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 | a0001c0001t0001g0107 | 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 | 1 | a0001c0001t0001g0169 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-356-1425C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 1/16 | chrX | 38032109 | |||||||
| chrX:38032363 | A | T | 51 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(48): 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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 1 | a0001c0001t0003g0006 | 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | a0001c0004t0003g0233 | 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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:38033186 | T | C | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | a0001c0002t0021g0024 a0001c0004t0002g0030 a0002c0003t0006g0028 others(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 | a0001c0001t0001g0086 a0001c0001t0001g0151 a0001c0001t0001g0212 others(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: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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0003c0005t0003g0234 | 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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | a0001c0002t0002g0071 | 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 | 107 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(104): Show |
113 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(110): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0001g0186 | 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 | a0001c0001t0019g0042 a0001c0002t0002g0040 a0001c0002t0002g0041 others(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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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:38037788 | T | A | 1 | a0001c0002t0002g0059 | 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 | 59 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0080 others(56): Show |
63 | HG00544.hp2 HG00558.hp1 HG00673.hp1 others(60): 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 | a0001c0001t0001g0083 a0001c0001t0001g0100 a0001c0001t0001g0140 others(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 | a0001c0001t0001g0106 a0001c0002t0002g0241 a0001c0002t0004g0091 others(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 | a0001c0001t0001g0141 a0001c0002t0002g0071 |
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 | a0001c0001t0001g0154 a0001c0001t0001g0172 a0001c0001t0001g0173 others(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 | 22 | a0001c0001t0001g0180 a0001c0001t0001g0186 a0001c0001t0001g0204 others(19): 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 | a0001c0001t0001g0158 a0001c0001t0001g0166 |
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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0200 others(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:38037943 | C | T | 7 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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:38038251 | G | A | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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:38038329 | G | T | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | 18 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(15): Show |
19 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.119+4323T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038331 | |||||||
| chrX:38038367 | C | G | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0001t0001g0106 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.119+4495C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38038503 | |||||||
| chrX:38038912 | C | G | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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:38039865 | A | T | 86 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(83): 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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0001t0003g0219 | 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 | a0001c0001t0001g0147 | 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 | a0001c0002t0002g0241 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.119+6145G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040153 | |||||||
| chrX:38040173 | CA | C | 89 | a0001c0001t0001g0138 a0001c0001t0002g0013 a0001c0001t0005g0048 others(86): 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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | a0003c0005t0002g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.119+6406G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38040414 | |||||||
| chrX:38040455 | C | G | 1 | a0001c0001t0003g0104 | 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 | a0001c0001t0001g0148 | 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 | a0001c0001t0005g0065 | 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 | 46 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(43): 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0002g0232 others(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 | 59 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(56): 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 | 89 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(86): 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 | 52 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(49): 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 | 83 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(80): 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 | a0001c0004t0003g0233 a0001c0004t0004g0227 a0001c0004t0004g0228 others(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 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0016 |
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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0204 | 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0001t0001g0100 | 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 | a0001c0001t0014g0175 | 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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:38043283 | A | G | 14 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | 52 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(49): 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 | G | 17 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(14): Show |
18 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(15): 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 | a0001c0001t0001g0150 a0001c0001t0001g0152 a0001c0001t0001g0153 others(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 | a0001c0001t0001g0100 a0001c0001t0001g0103 a0001c0001t0001g0151 others(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 | a0001c0001t0001g0121 a0001c0001t0001g0222 a0003c0005t0002g0058 |
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 | a0001c0001t0001g0072 a0001c0001t0001g0080 a0001c0004t0003g0233 others(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 | a0001c0001t0001g0127 a0001c0001t0001g0148 a0002c0003t0002g0046 |
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 | a0001c0001t0001g0076 a0001c0001t0001g0107 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0074 a0001c0001t0001g0077 a0001c0001t0001g0081 others(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 | a0001c0001t0001g0073 a0001c0001t0001g0079 a0001c0001t0001g0116 others(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 | a0001c0001t0001g0125 a0001c0001t0001g0143 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0111 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0136 a0001c0001t0001g0138 a0001c0004t0004g0229 others(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 | a0001c0001t0001g0126 a0006c0009t0001g0096 |
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 | a0001c0001t0001g0140 | 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 | a0001c0002t0021g0024 a0001c0004t0002g0030 a0002c0003t0007g0025 others(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 | 41 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(38): 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 | a0001c0001t0001g0200 a0001c0001t0003g0242 a0002c0003t0004g0199 |
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 | a0001c0001t0006g0037 | 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 | a0003c0005t0004g0230 | 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 | a0001c0001t0001g0122 | 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0005g0051 a0001c0004t0002g0020 a0003c0005t0002g0010 |
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 | 24 | a0001c0001t0005g0048 a0001c0001t0005g0055 a0001c0001t0005g0056 others(21): 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 | a0001c0002t0002g0033 a0001c0002t0002g0050 a0001c0002t0002g0236 others(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: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 | 6 | a0001c0002t0002g0003 a0001c0002t0002g0145 a0001c0002t0002g0232 others(3): 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 | 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 |
9 | a0001c0001t0001g0086 a0002c0003t0004g0004 a0002c0003t0004g0085 others(6): Show |
10 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(7): 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 | a0001c0002t0004g0091 a0001c0004t0004g0092 a0002c0003t0004g0087 others(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 | a0001c0002t0002g0047 a0001c0002t0020g0045 a0001c0004t0002g0049 |
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 | a0001c0002t0002g0053 a0001c0002t0002g0060 a0001c0002t0002g0061 others(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 | a0001c0004t0006g0171 a0001c0004t0023g0023 |
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:38044112 | C | T | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | a0001c0001t0003g0198 a0001c0001t0003g0242 |
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 | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | 47 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(44): 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0004t0003g0233 | 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 | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0002t0002g0060 | 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 | a0001c0001t0006g0037 a0001c0004t0002g0049 a0002c0003t0002g0044 others(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: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:38045569 | T | G | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | a0001c0001t0001g0120 | 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 | a0002c0003t0004g0199 | 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 | 47 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(44): 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:38046292 | C | T | 1 | a0001c0004t0003g0233 | 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 | 107 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(104): Show |
113 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(110): 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 | a0001c0001t0001g0110 | 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 | 84 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(81): 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 | 47 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(44): 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 | 107 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(104): Show |
113 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(110): 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0002t0002g0052 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0002g0232 others(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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0001t0001g0153 a0001c0004t0006g0171 a0001c0004t0023g0023 |
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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0003c0005t0002g0010 | 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 | 188 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(185): Show |
195 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.120-6830A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38047383 | |||||||
| chrX:38047422 | G | A | 82 | a0001c0001t0002g0013 a0001c0001t0005g0048 a0001c0001t0005g0051 others(79): 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0001t0003g0176 a0001c0001t0003g0197 |
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 | a0001c0001t0005g0051 | 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 | a0001c0001t0003g0184 a0001c0001t0003g0185 |
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 | a0001c0001t0001g0112 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.120-6033C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048180 | |||||||
| chrX:38048192 | A | G | 1 | a0001c0004t0003g0233 | 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 | a0003c0005t0003g0234 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0002g0232 others(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 | CA | C | 66 | a0001c0001t0001g0072 a0001c0001t0001g0086 a0001c0001t0001g0115 others(63): Show |
70 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(67): Show |
intron_variant | MODIFIER | c.120-5670delA | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | INFO_REALIGN_3_PRIME | chrX | 38048527 | ||||||
| chrX:38048601 | A | G | 2 | a0001c0001t0001g0123 a0001c0001t0001g0142 |
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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | 102 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(99): Show |
108 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(105): 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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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:38048736 | T | G | 1 | a0001c0002t0002g0237 | 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 | a0001c0002t0002g0237 | 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 | 100 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(97): Show |
106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): Show |
intron_variant | MODIFIER | c.120-5467C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38048746 | |||||||
| chrX:38049036 | A | C | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0001t0003g0009 | 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 | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-4839A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38049374 | |||||||
| chrX:38049474 | A | G | 47 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(44): 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 | a0001c0001t0003g0009 | 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 | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): 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 | a0001c0002t0021g0024 a0001c0004t0002g0030 a0002c0003t0006g0028 others(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 | a0001c0001t0003g0211 | 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0004t0002g0011 | 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 | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-3788G>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050425 | |||||||
| chrX:38050631 | C | T | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-3582C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050631 | |||||||
| chrX:38050657 | G | A | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.120-3556G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050657 | |||||||
| chrX:38050796 | T | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-3417T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050796 | |||||||
| chrX:38050797 | T | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): Show |
intron_variant | MODIFIER | c.120-3416T>C | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050797 | |||||||
| chrX:38050813 | G | A | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.120-3400G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38050813 | |||||||
| chrX:38050857 | G | C | 101 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(98): Show |
107 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(104): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0002t0002g0235 a0001c0002t0002g0236 a0001c0002t0002g0237 |
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 | a0001c0002t0002g0017 | 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 | a0001c0001t0001g0148 | 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 | a0003c0005t0003g0234 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0004t0002g0070 others(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 | a0001c0004t0004g0227 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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 | a0001c0004t0003g0233 a0003c0005t0003g0234 |
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 | a0001c0001t0003g0208 | 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 | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | a0001c0001t0001g0202 | 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 | a0003c0005t0003g0234 | 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 | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0001t0004g0005 | 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 | 17 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0002t0004g0091 others(14): Show |
18 | HG00733.hp1 HG01167.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.120-1154G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 2/16 | chrX | 38053059 | |||||||
| chrX:38053583 | G | C | 47 | a0001c0001t0005g0048 a0001c0001t0005g0051 a0001c0001t0005g0055 others(44): 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 | a0003c0005t0002g0058 | 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 | a0001c0001t0003g0208 | 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 | a0001c0002t0002g0069 | 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 | 16 | a0001c0001t0001g0180 a0001c0001t0001g0204 a0001c0001t0003g0006 others(13): 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 | GGT | G | 151 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0001g0172 others(148): Show |
158 | HG00099.hp2 HG00544.hp2 HG00558.hp1 others(155): 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 | a0001c0004t0004g0227 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0111 a0001c0001t0001g0119 others(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 | a0001c0001t0001g0076 a0001c0001t0001g0079 a0001c0001t0001g0083 others(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 | 53 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0180 others(50): 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 | TGAGAGA | T | 5 | a0001c0001t0003g0099 a0001c0002t0004g0091 a0001c0004t0004g0092 others(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 | 61 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0005g0048 others(58): Show |
65 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(62): 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 | a0001c0001t0002g0013 a0001c0002t0002g0014 a0001c0002t0002g0015 others(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 | 99 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(96): Show |
105 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(102): 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 | a0001c0002t0002g0031 a0001c0002t0002g0033 a0001c0002t0002g0232 others(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 | a0001c0004t0004g0227 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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 | 100 | a0001c0001t0001g0086 a0001c0001t0001g0169 a0001c0001t0002g0013 others(97): Show |
106 | HG00544.hp2 HG00558.hp1 HG00639.hp2 others(103): 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 | a0001c0002t0021g0024 | 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 | a0001c0002t0002g0017 | 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 | a0001c0002t0004g0129 | 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 | a0001c0004t0002g0231 | 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 | 44 | a0001c0001t0001g0169 a0001c0001t0004g0168 a0001c0002t0002g0232 others(41): Show |
47 | HG00642.hp1 HG00733.hp1 HG01167.hp1 others(44): 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 | a0001c0001t0003g0185 | 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 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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:38057124 | A | T | 1 | a0001c0002t0002g0216 | 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 | 103 | a0001c0001t0002g0013 a0001c0001t0004g0168 a0001c0002t0002g0002 others(100): 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0004t0002g0231 | 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 | a0001c0001t0001g0158 a0001c0001t0001g0166 |
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 | 72 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(69): 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 | a0001c0004t0002g0008 a0001c0004t0002g0231 a0001c0004t0004g0227 others(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 | a0001c0004t0002g0008 | 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:38058357 | T | A | 7 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0002c0003t0004g0004 a0002c0003t0004g0085 a0002c0003t0004g0087 others(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 | a0001c0001t0001g0201 | 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | 43 | a0001c0001t0001g0140 a0001c0002t0002g0002 a0001c0002t0002g0007 others(40): 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 | 80 | a0001c0001t0001g0140 a0001c0002t0002g0002 a0001c0002t0002g0003 others(77): 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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: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:38060142 | T | A | 1 | a0003c0005t0002g0032 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0002c0003t0004g0085 a0002c0003t0004g0093 |
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 | 80 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(77): 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 | a0001c0004t0002g0070 | 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 | 30 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(27): 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 | a0001c0001t0001g0172 a0001c0001t0001g0173 a0001c0001t0001g0201 |
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 | a0001c0002t0002g0240 | 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 | a0001c0002t0002g0050 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0010g0021 others(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 | 80 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(77): 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 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0136 |
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 | 73 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(70): 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 | a0003c0005t0003g0234 | 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:38061390 | A | G | 7 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0004t0004g0228 a0001c0004t0004g0229 a0001c0004t0017g0226 others(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 | 81 | a0001c0001t0003g0108 a0001c0002t0002g0002 a0001c0002t0002g0003 others(78): 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 | 77 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(74): 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 | a0001c0001t0002g0013 | 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 | a0001c0002t0004g0091 a0001c0004t0004g0092 a0002c0003t0002g0239 others(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 | a0001c0001t0001g0100 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.329+7445C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38061867 | |||||||
| chrX:38062002 | C | G | 2 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0002t0002g0059 | 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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0014 others(39): 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 | 9 | a0001c0002t0002g0003 a0001c0002t0002g0241 a0003c0005t0002g0001 others(6): 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 | a0001c0001t0012g0156 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.329+8297T>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 3/16 | chrX | 38062719 | |||||||
| chrX:38063089 | G | GT | 41 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0014 others(38): 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:38064058 | CAT | C | 17 | a0001c0004t0004g0227 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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:38064067 | A | G | 2 | a0001c0004t0002g0008 a0001c0004t0002g0238 |
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 | 70 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(67): 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:38064225 | G | A | 5 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0058 others(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:38064443 | G | T | 1 | a0003c0005t0002g0058 | 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 | a0001c0002t0004g0091 a0001c0004t0004g0092 a0002c0003t0002g0066 others(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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0014 others(39): 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 | 78 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(75): 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 | a0001c0001t0001g0076 a0001c0001t0001g0081 a0001c0001t0001g0107 others(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:38065377 | AT | A | 5 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0058 others(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 | 87 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(84): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(85): 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 | a0003c0005t0002g0032 a0003c0005t0003g0234 |
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 | T | 2 | a0001c0001t0001g0126 a0001c0001t0003g0108 |
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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0184 others(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:38066134 | A | C | 1 | a0003c0007t0006g0068 | 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 | a0001c0004t0004g0227 | 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 | a0001c0002t0004g0091 a0002c0003t0002g0044 a0002c0003t0002g0046 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 75 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(72): 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 | a0001c0001t0003g0220 a0001c0001t0003g0225 |
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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0058 |
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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0008t0004g0101 | 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 | a0001c0002t0002g0240 | 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 | 33 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(30): 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:38067387 | A | G | 4 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0002t0002g0145 | 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 | 25 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(22): 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0001t0001g0086 a0001c0001t0001g0106 |
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 | 4 | a0001c0002t0002g0002 a0001c0002t0002g0038 a0001c0002t0002g0039 others(1): 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 | a0001c0001t0001g0137 | 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 | 25 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(22): 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 | a0001c0001t0002g0013 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0002t0002g0071 | 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 | a0001c0001t0003g0205 a0001c0001t0014g0175 |
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 | 72 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(69): 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 | a0001c0004t0010g0022 | 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 | a0001c0002t0002g0240 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 33 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0016 others(30): 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 | a0001c0002t0002g0017 | 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:38070699 | A | G | 1 | a0001c0004t0004g0227 | 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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0014 others(39): 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 | a0001c0004t0004g0228 a0001c0004t0004g0229 |
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:38071055 | T | C | 1 | a0001c0002t0002g0059 | 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 | 79 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(76): 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0004t0002g0070 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0002c0003t0004g0160 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 42 | a0001c0002t0002g0002 a0001c0002t0002g0007 a0001c0002t0002g0014 others(39): 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 | a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0004t0023g0023 | 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 | 80 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(77): 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 | a0001c0004t0003g0233 | 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0002t0002g0240 | 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 | 5 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(2): 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 | a0001c0002t0002g0237 | 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 | a0001c0008t0004g0101 | 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 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(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 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0010g0021 others(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 | 4 | a0001c0001t0001g0110 a0001c0001t0001g0119 a0001c0001t0001g0169 others(1): Show |
4 | HG00099.hp1 HG01074.hp1 HG01361.hp2 others(1): 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 | a0001c0002t0002g0240 | 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 | a0001c0002t0002g0240 | 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 | 1 | a0001c0001t0003g0006 | 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 | a0001c0001t0001g0143 a0001c0001t0003g0099 a0001c0001t0003g0177 others(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 | 81 | a0001c0001t0001g0086 a0001c0001t0001g0106 a0001c0001t0003g0194 others(78): 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 | a0001c0002t0002g0240 a0003c0005t0002g0032 |
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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0002t0002g0240 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 2 | a0001c0002t0002g0003 a0001c0002t0002g0241 |
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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0003c0005t0003g0234 | 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 | 80 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(77): 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 | a0001c0001t0003g0242 | 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 | a0002c0003t0004g0004 a0002c0003t0004g0087 a0002c0003t0004g0088 others(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 | 80 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(77): 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 | a0001c0002t0002g0053 | 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 | 44 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(41): 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 | a0001c0001t0001g0125 | 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 | a0001c0001t0001g0120 | 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 | 99 | a0001c0001t0002g0013 a0001c0001t0004g0168 a0001c0002t0002g0002 others(96): 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 | a0003c0005t0003g0234 | 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 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0002g0238 others(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 | a0001c0001t0001g0201 a0003c0005t0002g0001 a0003c0005t0002g0010 others(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:38077910 | A | G | 1 | a0001c0002t0002g0240 | 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 | a0001c0001t0004g0188 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.689+1221C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38077922 | |||||||
| 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 | a0001c0004t0002g0008 a0001c0004t0004g0092 a0001c0004t0004g0227 others(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 | 79 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(76): 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 | a0001c0001t0003g0009 | 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 | a0001c0001t0001g0102 | 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 | a0001c0004t0023g0023 | 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 | a0001c0001t0001g0148 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.689+1839G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 6/16 | chrX | 38078540 | |||||||
| chrX:38078693 | G | A | 8 | a0001c0004t0002g0008 a0001c0004t0002g0231 a0001c0004t0004g0092 others(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 | a0001c0001t0001g0159 | 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0001t0001g0222 | 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 | a0001c0001t0001g0133 | 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 | a0001c0002t0002g0240 a0002c0003t0002g0044 a0002c0003t0002g0046 others(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 | a0001c0001t0008g0097 a0001c0001t0008g0098 a0001c0001t0019g0042 |
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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0002t0002g0039 a0001c0002t0004g0078 |
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:38079301 | G | A | 2 | a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0002t0002g0053 | 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 | a0001c0002t0002g0240 a0002c0003t0002g0044 a0002c0003t0002g0046 others(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 | a0001c0001t0003g0210 a0001c0001t0003g0213 |
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:38080487 | A | G | 81 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(78): 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:38080992 | A | C | 4 | a0001c0002t0002g0016 a0001c0002t0002g0033 a0001c0002t0002g0071 others(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:38081017 | G | A | 7 | a0001c0004t0002g0008 a0001c0004t0004g0092 a0001c0004t0004g0227 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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: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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 5 | a0001c0002t0002g0003 a0001c0002t0002g0031 a0001c0002t0002g0232 others(2): 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0005c0011t0003g0190 | 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | 97 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(94): 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | 81 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(78): 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | a0001c0002t0002g0031 | 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 | a0001c0001t0001g0110 | 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 | a0002c0003t0006g0028 a0002c0003t0006g0029 |
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 | 73 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(70): 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 | a0001c0001t0004g0005 | 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 | a0001c0002t0002g0047 a0001c0002t0002g0061 a0001c0002t0002g0062 others(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 | a0002c0003t0002g0239 a0002c0003t0006g0028 a0002c0003t0006g0029 others(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 | a0001c0001t0001g0172 a0001c0001t0001g0173 |
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 | 99 | a0001c0001t0002g0013 a0001c0001t0004g0168 a0001c0002t0002g0002 others(96): 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 |
1 | a0001c0002t0002g0007 | 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 | a0001c0002t0002g0214 | 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 | a0001c0004t0002g0008 a0002c0003t0002g0066 a0002c0003t0004g0167 others(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 | a0002c0003t0002g0239 a0002c0003t0004g0004 a0002c0003t0004g0085 others(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 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(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 |
28 | a0001c0001t0002g0013 a0001c0002t0002g0002 a0001c0002t0002g0003 others(25): 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 | a0001c0002t0002g0059 a0001c0002t0002g0237 a0001c0002t0020g0045 others(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 | a0001c0001t0004g0168 a0001c0002t0002g0038 a0001c0002t0004g0091 others(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 | a0001c0002t0002g0016 a0001c0002t0002g0031 a0001c0002t0002g0033 others(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 | a0001c0002t0002g0236 | 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 | 2 | a0001c0002t0002g0007 a0001c0002t0002g0214 |
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 | 27 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0075 others(24): Show |
27 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(24): 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 | 108 | a0001c0001t0001g0072 a0001c0001t0001g0076 a0001c0001t0001g0081 others(105): 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 | a0001c0001t0003g0157 a0001c0004t0004g0228 a0001c0004t0004g0229 others(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:38083809 | T | TGTGTGTG others(10): Show |
1 | a0001c0002t0002g0232 | 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 | 72 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(69): 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:38084019 | C | T | 2 | a0001c0001t0001g0112 a0001c0001t0001g0147 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0147 |
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 | a0001c0004t0002g0020 | 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 | a0003c0005t0003g0234 | 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 | 153 | a0001c0001t0001g0072 a0001c0001t0001g0132 a0001c0001t0001g0172 others(150): 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:38085340 | A | G | 6 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 46 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(43): 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 | 46 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(43): 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:38086632 | T | C | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | a0003c0005t0003g0234 | 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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0116 a0001c0001t0001g0162 |
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 | a0001c0008t0004g0101 | 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 | a0003c0005t0002g0058 | 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | a0001c0001t0001g0200 | 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 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0010g0021 others(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 | a0001c0001t0001g0100 | 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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | 78 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(75): 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 | a0001c0001t0001g0135 | 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 | a0001c0002t0002g0038 | 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 | a0001c0001t0001g0222 | 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 | a0001c0001t0003g0219 a0001c0001t0014g0175 |
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 | a0002c0003t0004g0004 a0002c0003t0004g0087 a0002c0003t0004g0088 others(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 | a0001c0004t0002g0020 | 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 | 77 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(74): 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 | 2 | a0001c0002t0002g0003 a0001c0002t0002g0241 |
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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0001t0001g0115 a0001c0001t0001g0122 |
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 | a0001c0004t0004g0092 a0001c0004t0004g0227 a0003c0005t0002g0001 others(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 | a0001c0001t0003g0211 | 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 | a0001c0002t0002g0145 | 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 | 99 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(96): 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 | 2 | a0001c0002t0002g0002 a0001c0002t0002g0038 |
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 | a0001c0001t0003g0220 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0001t0005g0065 | 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0111 | 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 | a0001c0001t0001g0102 | 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 | a0001c0001t0004g0188 | 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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | a0001c0001t0001g0124 | 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:38094550 | T | C | 1 | a0001c0001t0004g0188 | 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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0001t0003g0224 | 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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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:38096674 | G | C | 2 | a0002c0003t0006g0028 a0002c0003t0006g0029 |
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 | a0001c0002t0002g0038 | 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0001t0003g0131 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1062+715C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38096949 | |||||||
| chrX:38097188 | G | A | 1 | a0001c0002t0002g0145 | 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 | a0001c0001t0003g0194 a0001c0001t0003g0198 a0001c0001t0003g0242 others(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 | a0003c0005t0002g0010 a0003c0005t0002g0032 |
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:38097847 | A | G | 7 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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: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 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0010g0021 others(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 | a0001c0004t0002g0011 a0001c0004t0002g0012 a0001c0004t0002g0030 others(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 | a0001c0002t0002g0240 | 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 | a0001c0001t0001g0115 | 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 | a0002c0003t0004g0004 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | 13 | a0001c0001t0001g0132 a0001c0001t0001g0186 a0001c0001t0003g0006 others(10): 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0002t0002g0240 | 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 | 101 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(98): 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 | a0001c0001t0001g0073 a0001c0001t0001g0074 a0001c0001t0001g0077 others(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 | a0001c0002t0004g0129 | 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 | a0001c0008t0004g0101 | 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 | a0001c0001t0001g0202 | 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 | a0001c0002t0002g0050 | 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0004t0002g0231 | 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 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 others(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 | 103 | a0001c0001t0002g0013 a0001c0001t0004g0168 a0001c0002t0002g0002 others(100): 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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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 | a0001c0001t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1063-742A>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 9/16 | chrX | 38101600 | |||||||
| chrX:38101681 | GTA | G | 7 | a0001c0004t0002g0020 a0001c0004t0002g0070 a0001c0004t0002g0238 others(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 | a0001c0004t0002g0008 | 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 | CA | C | 83 | a0001c0001t0001g0126 a0001c0001t0001g0127 a0001c0001t0001g0137 others(80): 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 | a0001c0002t0004g0178 a0003c0005t0002g0001 a0003c0005t0002g0010 others(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:38101978 | T | C | 24 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0003c0005t0002g0001 a0003c0005t0002g0010 a0003c0005t0002g0032 others(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:38102259 | TGAAA | T | 24 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0001c0004t0004g0228 a0001c0004t0004g0229 a0001c0004t0017g0226 others(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 | a0001c0001t0004g0188 | 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 | a0001c0004t0004g0228 a0001c0004t0004g0229 a0001c0004t0017g0226 others(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 | a0003c0005t0003g0234 | 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 | 77 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(74): 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 | a0001c0002t0002g0237 | 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 | a0001c0001t0003g0155 a0001c0001t0003g0157 a0001c0001t0003g0184 others(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 | a0001c0002t0002g0240 | 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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0001c0001t0001g0136 | 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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0002t0002g0017 a0001c0002t0002g0018 a0001c0002t0002g0019 |
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 | 77 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(74): 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 | a0001c0001t0002g0013 a0001c0001t0004g0168 |
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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0001c0001t0014g0175 | 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 | a0003c0005t0002g0032 | 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 | a0001c0004t0002g0011 a0001c0004t0002g0012 a0001c0004t0002g0030 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0001t0001g0103 a0001c0001t0001g0121 a0001c0001t0001g0130 others(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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0001c0004t0004g0227 | 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 | 78 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(75): 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 | a0001c0002t0002g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1156-414C>G | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 10/16 | chrX | 38106179 | |||||||
| chrX:38106914 | C | T | 1 | a0001c0001t0001g0111 | 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 | a0002c0003t0004g0004 a0002c0003t0004g0087 a0002c0003t0004g0088 others(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 | 78 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(75): 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 | 50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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:38108983 | G | A | 1 | a0003c0007t0006g0068 | 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 | a0001c0004t0004g0228 a0001c0004t0004g0229 a0001c0004t0017g0226 others(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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0001c0004t0004g0228 a0001c0004t0004g0229 a0001c0004t0017g0226 others(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 | a0001c0001t0003g0185 | 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 | a0001c0002t0002g0240 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1435-569C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 12/16 | chrX | 38109752 | |||||||
| chrX:38109770 | C | G | 27 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | a0001c0002t0002g0053 | 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | a0001c0004t0003g0233 a0001c0004t0006g0171 |
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 | a0002c0003t0018g0206 | 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 | a0001c0001t0001g0103 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | 2 | a0001c0002t0002g0002 a0001c0002t0002g0038 |
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 | a0001c0004t0002g0008 | 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 | a0001c0001t0001g0150 a0001c0001t0001g0151 a0001c0001t0001g0152 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0134 |
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 | a0001c0004t0002g0008 a0001c0004t0004g0092 a0001c0004t0004g0227 others(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 | a0001c0004t0002g0020 | 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 | a0001c0001t0003g0225 | 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 |
50 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(47): 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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | a0002c0003t0004g0160 | 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 | a0003c0005t0003g0234 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 |
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 | a0001c0001t0012g0156 | 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 | a0001c0004t0002g0238 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1596+2677C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 13/16 | chrX | 38113159 | |||||||
| chrX:38113421 | T | A | 1 | a0001c0001t0003g0198 | 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 others(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 | 85 | a0001c0002t0002g0002 a0001c0002t0002g0003 a0001c0002t0002g0007 others(82): 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 | a0001c0001t0014g0175 | 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 | 86 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0002t0002g0002 others(83): 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0003g0009 a0001c0001t0003g0104 a0001c0001t0003g0108 others(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 | a0004c0006t0001g0139 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | a0001c0002t0002g0064 | 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 | a0001c0004t0002g0020 a0001c0004t0002g0030 a0001c0004t0002g0070 others(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 | a0001c0001t0003g0219 a0001c0001t0014g0175 |
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 | 49 | a0001c0001t0001g0072 a0001c0001t0001g0074 a0001c0001t0001g0111 others(46): Show |
50 | HG00621.hp1 HG00642.hp1 HG00673.hp1 others(47): 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 | CA | C | 11 | a0001c0001t0001g0125 a0001c0001t0001g0135 a0001c0001t0001g0166 others(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:38115709 | G | A | 1 | a0001c0002t0002g0237 | 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 | a0001c0001t0003g0211 | 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 | a0001c0004t0002g0231 | 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 | a0001c0002t0002g0014 a0001c0002t0002g0015 a0001c0002t0002g0060 others(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 | a0001c0002t0002g0040 a0001c0002t0002g0041 a0001c0002t0002g0043 others(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 | a0001c0001t0003g0099 | 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 | a0001c0001t0003g0207 a0001c0001t0003g0208 a0001c0001t0003g0210 others(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 | a0001c0004t0017g0226 a0001c0004t0022g0034 |
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 | 78 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(75): 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 | a0002c0003t0006g0028 | 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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | a0001c0002t0002g0031 a0001c0002t0002g0232 a0001c0002t0002g0236 others(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 | a0001c0004t0002g0020 a0001c0004t0002g0030 a0001c0004t0002g0070 others(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 | a0001c0001t0002g0013 | 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 | a0001c0001t0004g0168 a0003c0005t0002g0001 a0003c0005t0002g0010 others(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 | a0001c0002t0002g0240 | 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 | a0001c0001t0003g0185 | 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 | a0001c0001t0002g0013 | 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 | a0001c0001t0001g0127 a0001c0001t0001g0128 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0142 |
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 | a0001c0001t0002g0013 | 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 | a0001c0008t0004g0101 | 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 | a0001c0004t0002g0011 | 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 | a0001c0002t0002g0236 a0001c0002t0002g0240 a0001c0004t0002g0012 |
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 | a0001c0002t0002g0232 | 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 | a0001c0001t0001g0102 | 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 | a0001c0004t0010g0021 a0001c0004t0010g0022 |
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 | 130 | a0001c0001t0001g0072 a0001c0001t0001g0073 a0001c0001t0001g0074 others(127): Show |
131 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(128): 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 | 79 | a0001c0001t0003g0131 a0001c0001t0003g0219 a0001c0001t0004g0005 others(76): 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 | a0001c0001t0002g0013 | 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 | 19 | a0001c0001t0004g0168 a0001c0001t0004g0195 a0001c0002t0002g0002 others(16): 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 | a0001c0001t0004g0168 a0001c0002t0002g0017 a0001c0002t0002g0018 others(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 | 13 | a0001c0001t0004g0195 a0001c0002t0002g0002 a0001c0002t0002g0038 others(10): 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 | a0001c0001t0004g0168 a0001c0002t0002g0017 a0001c0002t0002g0018 others(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 | 13 | a0001c0001t0004g0195 a0001c0002t0002g0002 a0001c0002t0002g0038 others(10): 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 | 13 | a0001c0001t0004g0195 a0001c0002t0002g0002 a0001c0002t0002g0038 others(10): 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 | 19 | a0001c0001t0004g0168 a0001c0001t0004g0195 a0001c0002t0002g0002 others(16): 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 | a0001c0001t0004g0168 a0001c0002t0002g0017 a0001c0002t0002g0018 others(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 | a0001c0001t0001g0075 a0001c0001t0001g0172 a0001c0001t0001g0173 others(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 | 51 | a0001c0001t0004g0005 a0001c0002t0002g0003 a0001c0002t0002g0007 others(48): 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 | a0001c0002t0002g0014 | 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 | 19 | a0001c0001t0004g0168 a0001c0001t0004g0195 a0001c0002t0002g0002 others(16): 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:38118954 | T | TATATATA others(23): Show |
1 | a0001c0001t0006g0037 | 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 | a0001c0002t0002g0240 | 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 | a0001c0001t0005g0056 | 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 | a0001c0004t0002g0231 | 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 | a0001c0002t0002g0232 a0001c0002t0002g0236 a0001c0004t0002g0011 others(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 | a0001c0001t0003g0185 | 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 | 95 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(92): 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 | a0001c0002t0002g0059 | 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 | 69 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(66): 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 | a0001c0001t0001g0149 a0001c0002t0002g0145 |
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 | a0001c0002t0002g0216 | 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 | a0001c0001t0001g0114 a0001c0001t0001g0143 |
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 | a0001c0002t0002g0031 a0001c0004t0002g0020 a0001c0004t0002g0070 others(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 | a0001c0001t0014g0175 | 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 | a0001c0002t0002g0232 a0001c0002t0002g0236 a0001c0002t0002g0240 others(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:38121602 | C | T | 1 | a0001c0004t0002g0231 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1706-478C>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121602 | |||||||
| chrX:38121678 | G | T | 7 | a0001c0004t0002g0008 a0001c0004t0017g0226 a0001c0004t0022g0034 others(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 | a0001c0002t0002g0145 | 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 | 2 | a0001c0002t0002g0003 a0001c0002t0002g0241 |
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 | a0001c0002t0004g0178 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1706-206C>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 14/16 | chrX | 38121874 | |||||||
| 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 | 95 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(92): 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 | a0001c0004t0002g0011 a0001c0004t0002g0012 a0001c0004t0002g0049 |
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 | a0001c0001t0001g0130 a0001c0001t0001g0141 |
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 | a0001c0004t0017g0226 a0001c0004t0022g0034 |
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 | a0001c0002t0002g0232 a0001c0002t0002g0236 a0001c0002t0002g0240 others(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:38122805 | C | T | 5 | a0001c0002t0002g0232 a0001c0002t0002g0236 a0001c0004t0002g0011 others(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 | a0001c0001t0008g0097 a0001c0001t0008g0098 a0001c0001t0019g0042 |
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 | a0001c0001t0001g0158 a0001c0001t0001g0166 |
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 | a0001c0002t0002g0061 | 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 | a0001c0001t0003g0009 | 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 | a0001c0008t0004g0101 | 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 | a0001c0001t0002g0013 | 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 | a0003c0005t0002g0058 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1841+1420G>T | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38123635 | |||||||
| chrX:38124042 | G | A | 1 | a0001c0001t0001g0102 | 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 | a0001c0001t0001g0126 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1842-936G>A | SYTL5 | ENSG00000147041.12 | transcript | ENST00000297875.7 | protein_coding | 15/16 | chrX | 38124362 | |||||||
| chrX:38124553 | A | T | 87 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(84): 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 | a0002c0003t0002g0044 a0002c0003t0002g0046 a0002c0003t0002g0057 |
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 | a0001c0004t0002g0231 | 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 | 87 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(84): 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 | a0001c0004t0004g0227 | 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 | 88 | a0001c0001t0004g0005 a0001c0001t0004g0168 a0001c0001t0004g0195 others(85): 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 | a0001c0001t0001g0115 a0001c0001t0001g0116 a0001c0001t0001g0122 others(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 |