Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 6853 |
| ensemblid | ENSG00000008056.14 |
| hgncid | 11494 |
| symbol | SYN1 |
| name | synapsin I |
| refseq_nuc | NM_006950.3 |
| refseq_prot | NP_008881.2 |
| ensembl_nuc | ENST00000295987.13 |
| ensembl_prot | ENSP00000295987.7 |
| mane_status | MANE Select |
| chr | chrX |
| start | 47571901 |
| end | 47619857 |
| strand | - |
| ver | v1.2 |
| region | chrX:47571901-47619857 |
| region5000 | chrX:47566901-47624857 |
| regionname0 | SYN1_chrX_47571901_47619857 |
| regionname5000 | SYN1_chrX_47566901_47624857 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 705 | 275 | 74 | 53 | 109 | 11 | 26 | 82 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| a0002 | 0/0 | 705 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| a0003 | 0/0 | 705 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| a0004 | 0/0 | 700 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(695): Show |
chrX | 47566901 | 47624857 |
| a0005 | 0/0 | 705 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| a0006 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| a0007 | 0/0 | 705 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | MNYLR others(700): Show |
chrX | 47566901 | 47624857 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 2115 | 179 | 33 | 32 | 86 | 7 | 19 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0001c0002 | 0/0 | 2115 | 89 | 38 | 19 | 22 | 4 | 6 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0001c0003 | 0/0 | 2115 | 4 | 3 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0001c0009 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0001c0010 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0001c0011 | 0/0 | 2115 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0002c0004 | 0/0 | 2115 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0003c0005 | 0/0 | 2115 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0004c0012 | 0/0 | 2100 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2095): Show |
chrX | 47566901 | 47624857 | ||
| a0005c0007 | 0/0 | 2115 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0006c0006 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 | ||
| a0007c0008 | 0/0 | 2115 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | ATGAA others(2110): Show |
chrX | 47566901 | 47624857 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 3210 | 178 | 32 | 32 | 86 | 7 | 19 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0001t0004 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0002t0001 | 0/0 | 3210 | 85 | 35 | 18 | 22 | 4 | 6 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0002t0002 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0002t0003 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0002t0005 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0003t0001 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0003t0002 | 0/0 | 3210 | 2 | 1 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0009t0001 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0010t0001 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0001c0011t0001 | 0/0 | 3210 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0002c0004t0001 | 0/0 | 3210 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0003c0005t0001 | 0/0 | 3210 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0004c0012t0001 | 0/0 | 3195 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3190): Show |
chrX | 47566901 | 47624857 |
| a0005c0007t0001 | 0/0 | 3210 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0006c0006t0001 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| a0007c0008t0001 | 0/0 | 3210 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | AGTCT others(3205): Show |
chrX | 47566901 | 47624857 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 8 | 0 | 6 | 2 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0002 | 0/0 | 7 | 0 | 2 | 1 | 0 | 4 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0007 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0001t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0003 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0002g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0003g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0002t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0003t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0003t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0003t0002g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0009t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0010t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0001c0011t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0002c0004t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0002c0004t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0003c0005t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0004c0012t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0005c0007t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0006c0006t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| a0007c0008t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0001 | g0072 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0063 | EUR | GBR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0154 | EUR | FIN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00408 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00408 | hp2 | a0001 | c0002 | t0001 | g0246 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00438 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00544 | hp1 | a0001 | c0002 | t0001 | g0036 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00544 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00597 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00597 | hp2 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00609 | hp1 | a0001 | c0002 | t0001 | g0248 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00733 | hp1 | a0001 | c0002 | t0001 | g0232 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00733 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00735 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00735 | hp2 | a0001 | c0003 | t0002 | g0212 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00738 | hp1 | a0001 | c0002 | t0001 | g0018 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00741 | hp1 | a0001 | c0002 | t0001 | g0237 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG00741 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01069 | hp1 | a0001 | c0002 | t0001 | g0238 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01070 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0047 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0090 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01109 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0207 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01243 | hp1 | a0001 | c0009 | t0001 | g0150 | AMR | PUR | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0252 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01258 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01261 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01346 | hp1 | a0001 | c0002 | t0001 | g0069 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01358 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01361 | hp1 | a0001 | c0002 | t0001 | g0256 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01433 | hp1 | a0001 | c0002 | t0001 | g0236 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01496 | hp1 | a0001 | c0002 | t0001 | g0239 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01496 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01515 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0211 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01517 | hp2 | a0001 | c0002 | t0001 | g0210 | EUR | IBS | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01884 | hp2 | a0001 | c0003 | t0001 | g0014 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01891 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01891 | hp2 | a0001 | c0002 | t0001 | g0015 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0032 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01934 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01943 | hp1 | a0001 | c0002 | t0001 | g0241 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01952 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01978 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0247 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01993 | hp1 | a0001 | c0002 | t0001 | g0034 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01993 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0234 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02027 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02040 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02055 | hp1 | a0001 | c0002 | t0001 | g0017 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02071 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02129 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02135 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02145 | hp1 | a0001 | c0002 | t0001 | g0042 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02148 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02148 | hp2 | a0001 | c0002 | t0005 | g0233 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0223 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02257 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02273 | hp1 | a0001 | c0002 | t0001 | g0235 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02273 | hp2 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02293 | hp1 | a0003 | c0005 | t0001 | g0203 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PEL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02451 | hp1 | a0001 | c0002 | t0001 | g0024 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02572 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02622 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02630 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02630 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0167 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02717 | hp1 | a0001 | c0003 | t0002 | g0214 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02723 | hp1 | a0001 | c0002 | t0002 | g0011 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02723 | hp2 | a0001 | c0002 | t0001 | g0019 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02735 | hp1 | a0001 | c0011 | t0001 | g0243 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02809 | hp1 | a0001 | c0002 | t0002 | g0012 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0190 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02818 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02818 | hp2 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02886 | hp1 | a0001 | c0002 | t0001 | g0022 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02886 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02896 | hp1 | a0001 | c0001 | t0001 | g0195 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02896 | hp2 | a0001 | c0001 | t0001 | g0159 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02897 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02922 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02922 | hp2 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02970 | hp1 | a0001 | c0002 | t0001 | g0003 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02970 | hp2 | a0001 | c0002 | t0001 | g0016 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02976 | hp1 | a0001 | c0001 | t0004 | g0198 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02976 | hp2 | a0001 | c0002 | t0001 | g0218 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03041 | hp1 | a0001 | c0002 | t0001 | g0029 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03041 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03098 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03130 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03139 | hp1 | a0001 | c0002 | t0003 | g0010 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03195 | hp1 | a0001 | c0002 | t0001 | g0039 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03195 | hp2 | a0001 | c0002 | t0001 | g0028 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03209 | hp1 | a0001 | c0002 | t0001 | g0219 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03225 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03453 | hp1 | a0001 | c0002 | t0001 | g0041 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03453 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03486 | hp1 | a0001 | c0002 | t0001 | g0255 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03486 | hp2 | a0001 | c0001 | t0001 | g0193 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0228 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03516 | hp1 | a0002 | c0004 | t0001 | g0258 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03516 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ESN | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03540 | hp1 | a0001 | c0002 | t0001 | g0027 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03540 | hp2 | a0002 | c0004 | t0001 | g0259 | AFR | GWD | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03579 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03654 | hp1 | a0001 | c0002 | t0001 | g0070 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03704 | hp2 | a0001 | c0002 | t0001 | g0035 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03831 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03831 | hp2 | a0001 | c0002 | t0001 | g0226 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0173 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0148 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03927 | hp1 | a0001 | c0002 | t0001 | g0251 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG04199 | hp1 | a0001 | c0001 | t0001 | g0093 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG04228 | hp1 | a0001 | c0002 | t0001 | g0225 | SAS | STU | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18522 | hp1 | a0001 | c0002 | t0001 | g0221 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18612 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | CHB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18747 | hp1 | a0001 | c0002 | t0001 | g0250 | EAS | CHB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18906 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18940 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18942 | hp1 | a0004 | c0012 | t0001 | g0257 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18942 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18943 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18950 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18951 | hp2 | a0001 | c0002 | t0001 | g0030 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18952 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18953 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18959 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18960 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18964 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18966 | hp1 | a0001 | c0002 | t0001 | g0031 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18967 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18968 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18968 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18971 | hp1 | a0005 | c0007 | t0001 | g0117 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18974 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18979 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18979 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18983 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18986 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18987 | hp1 | a0001 | c0002 | t0001 | g0230 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18987 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18989 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18990 | hp1 | a0001 | c0010 | t0001 | g0129 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18992 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18992 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18998 | hp2 | a0001 | c0002 | t0001 | g0227 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0244 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19002 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19009 | hp1 | a0001 | c0002 | t0001 | g0009 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0224 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19030 | hp1 | a0001 | c0001 | t0001 | g0196 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19030 | hp2 | a0006 | c0006 | t0001 | g0046 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19043 | hp1 | a0007 | c0008 | t0001 | g0182 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19055 | hp1 | a0001 | c0002 | t0001 | g0204 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19056 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19063 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19065 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19068 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19072 | hp1 | a0001 | c0002 | t0001 | g0245 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19075 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19077 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19077 | hp2 | a0001 | c0002 | t0001 | g0229 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19081 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19081 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0249 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19085 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19086 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19088 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19089 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19240 | hp1 | a0001 | c0002 | t0001 | g0209 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA19240 | hp2 | a0001 | c0002 | t0001 | g0213 | AFR | YRI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA20752 | hp1 | a0001 | c0002 | t0001 | g0068 | EUR | TSI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA20805 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA20905 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | GIH | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01123 | hp1 | a0001 | c0002 | t0001 | g0242 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02109 | hp2 | a0001 | c0002 | t0001 | g0023 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0199 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG02559 | hp2 | a0001 | c0002 | t0001 | g0215 | AFR | ACB | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG03471 | hp1 | a0001 | c0002 | t0001 | g0026 | AFR | MSL | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| HG06807 | hp2 | a0001 | c0003 | t0001 | g0025 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA18955 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0071 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA20300 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | USA | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA21309 | hp1 | a0001 | c0002 | t0001 | g0073 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0131 | REF | REF | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0104 | REF | REF | SYN1_chrX_47566901_47624857 | SYN1 | chrX | 47566901 | 47624857 |
| 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:47574285 | T | C | 1 | a0002 | 2 | HG03516.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.1699A>G | p.Thr567Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1828/3210 | 1699/2118 | 567/705 | chrX | 47574285 | |||
| chrX:47574306 | G | T | 1 | a0005 | 1 | NA18971.hp1 | missense_variant | MODERATE | c.1678C>A | p.Pro560Thr | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1807/3210 | 1678/2118 | 560/705 | chrX | 47574306 | |||
| chrX:47574477 | G | C | 1 | a0007 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.1507C>G | p.Pro503Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/13 | 1636/3210 | 1507/2118 | 503/705 | chrX | 47574477 | |||
| chrX:47574756 | A | G | 1 | a0006 | 1 | NA19030.hp2 | missense_variant | MODERATE | c.1325T>C | p.Leu442Pro | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 11/13 | 1454/3210 | 1325/2118 | 442/705 | chrX | 47574756 | |||
| chrX:47576553 | C | T | 1 | a0003 | 1 | HG02293.hp1 | missense_variant | MODERATE | c.925G>A | p.Asp309Asn | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/13 | 1054/3210 | 925/2118 | 309/705 | chrX | 47576553 | |||
| chrX:47619396 | GGCTCCCC others(8): Show |
G | 1 | a0004 | 1 | NA18942.hp1 | disruptive_inframe_deletion | MODERATE | c.318_332delAGGCCGCG others(7): Show |
p.Gly107_Ala111del | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 461/3210 | 318/2118 | 106/705 | chrX | 47619396 | |||
| chrX:47619577 | G | C | 1 | a0002 | 2 | HG03516.hp1 HG03540.hp2 |
missense_variant | MODERATE | c.152C>G | p.Ala51Gly | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 281/3210 | 152/2118 | 51/705 | chrX | 47619577 |
| 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:47576566 | G | A | 2 | a0001c0003 a0001c0009 |
5 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(2): Show |
synonymous_variant | LOW | c.912C>T | p.Ala304Ala | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/13 | 1041/3210 | 912/2118 | 304/705 | chrX | 47576566 | |||
| chrX:47605014 | T | C | 1 | a0001c0010 | 1 | NA18990.hp1 | synonymous_variant | LOW | c.738A>G | p.Leu246Leu | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/13 | 867/3210 | 738/2118 | 246/705 | chrX | 47605014 | |||
| chrX:47606962 | A | G | 3 | a0001c0002 a0001c0003 a0001c0011 |
94 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(91): Show |
synonymous_variant | LOW | c.510T>C | p.Asn170Asn | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/13 | 639/3210 | 510/2118 | 170/705 | chrX | 47606962 | |||
| chrX:47607150 | T | C | 1 | a0001c0011 | 1 | HG02735.hp1 | synonymous_variant | LOW | c.426A>G | p.Lys142Lys | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 2/13 | 555/3210 | 426/2118 | 142/705 | chrX | 47607150 |
| 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:47572070 | A | G | 1 | a0001c0001t0004 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*794T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 794 | chrX | 47572070 | ||||||
| chrX:47572305 | G | A | 1 | a0001c0002t0005 | 1 | HG02148.hp2 | 3_prime_UTR_variant | MODIFIER | c.*559C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 559 | chrX | 47572305 | ||||||
| chrX:47572721 | C | T | 2 | a0001c0002t0002 a0001c0003t0002 |
4 | HG00735.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*143G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 13/13 | 143 | chrX | 47572721 | ||||||
| chrX:47619833 | A | T | 1 | a0001c0002t0003 | 1 | HG03139.hp1 | 5_prime_UTR_variant | MODIFIER | c.-105T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/13 | 105 | chrX | 47619833 |
| 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:47573348 | A | G | 142 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(139): Show |
149 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(146): Show |
intron_variant | MODIFIER | c.1983-349T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573348 | |||||||
| chrX:47573641 | C | CG | 17 | a0001c0001t0001g0051 a0001c0001t0001g0052 a0001c0001t0001g0103 others(14): Show |
17 | HG00438.hp2 HG00597.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.1982+360dupC | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573641 | |||||||
| chrX:47573666 | G | A | 1 | a0002c0004t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1982+336C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573666 | |||||||
| chrX:47573923 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1982+79C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 12/12 | chrX | 47573923 | |||||||
| chrX:47575306 | G | T | 1 | a0001c0001t0001g0165 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1159-32C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575306 | |||||||
| chrX:47575349 | T | C | 1 | a0001c0001t0001g0146 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1159-75A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575349 | |||||||
| chrX:47575795 | A | G | 1 | a0001c0001t0001g0108 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1158+336T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47575795 | |||||||
| chrX:47576006 | C | T | 2 | a0001c0002t0001g0070 a0001c0002t0001g0251 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1158+125G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47576006 | |||||||
| chrX:47576013 | T | C | 8 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0200 others(5): Show |
8 | HG01081.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1158+118A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 9/12 | chrX | 47576013 | |||||||
| chrX:47576240 | AGACAAAG | A | 4 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0002g0212 others(1): Show |
4 | HG00735.hp2 HG02717.hp1 HG02723.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1056-14_1056-8delC others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 8/12 | chrX | 47576240 | |||||||
| chrX:47576454 | G | A | 1 | a0001c0001t0001g0112 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.980+44C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 7/12 | chrX | 47576454 | |||||||
| chrX:47576648 | A | C | 7 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.838-8T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576648 | |||||||
| chrX:47576653 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.838-13C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47576653 | |||||||
| chrX:47577078 | C | T | 7 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.837+361G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577078 | |||||||
| chrX:47577179 | A | G | 8 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0200 others(5): Show |
8 | HG01081.hp1 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.837+260T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577179 | |||||||
| chrX:47577222 | A | G | 2 | a0001c0002t0001g0039 a0001c0002t0001g0223 |
2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.837+217T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 6/12 | chrX | 47577222 | |||||||
| chrX:47577624 | A | G | 7 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-123T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577624 | |||||||
| chrX:47577631 | A | G | 7 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-130T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577631 | |||||||
| chrX:47577638 | C | T | 1 | a0001c0002t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.775-137G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577638 | |||||||
| chrX:47577641 | G | A | 2 | a0001c0002t0001g0039 a0001c0002t0001g0223 |
2 | HG02257.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.775-140C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577641 | |||||||
| chrX:47577815 | G | A | 5 | a0001c0001t0001g0093 a0001c0001t0001g0132 a0001c0001t0001g0135 others(2): Show |
5 | HG01515.hp1 HG01517.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-314C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577815 | |||||||
| chrX:47577873 | G | T | 73 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(70): Show |
77 | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.775-372C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577873 | |||||||
| chrX:47577876 | G | C | 5 | a0001c0002t0001g0024 a0001c0002t0001g0070 a0001c0002t0001g0209 others(2): Show |
5 | HG02451.hp1 HG03486.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-375C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577876 | |||||||
| chrX:47577958 | A | C | 1 | a0001c0002t0001g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.775-457T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47577958 | |||||||
| chrX:47578127 | C | T | 7 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(4): Show |
7 | HG00735.hp2 HG01243.hp1 HG01884.hp2 others(4): Show |
intron_variant | MODIFIER | c.775-626G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578127 | |||||||
| chrX:47578220 | C | G | 3 | a0001c0003t0001g0014 a0001c0003t0001g0025 a0001c0009t0001g0150 |
3 | HG01243.hp1 HG01884.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.775-719G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578220 | |||||||
| chrX:47578372 | C | T | 12 | a0001c0001t0001g0051 a0001c0001t0001g0162 a0001c0001t0001g0163 others(9): Show |
12 | HG00741.hp1 HG01069.hp1 HG01346.hp1 others(9): Show |
intron_variant | MODIFIER | c.775-871G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578372 | |||||||
| chrX:47578431 | G | A | 2 | a0001c0001t0001g0161 a0001c0001t0001g0177 |
2 | NA19065.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.775-930C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578431 | |||||||
| chrX:47578649 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-1148C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578649 | |||||||
| chrX:47578721 | C | G | 2 | a0001c0002t0001g0070 a0001c0002t0001g0251 |
2 | HG03654.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.775-1220G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578721 | |||||||
| chrX:47578991 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-1490C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47578991 | |||||||
| chrX:47579068 | C | A | 2 | a0001c0003t0001g0014 a0001c0009t0001g0150 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.775-1567G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579068 | |||||||
| chrX:47579408 | T | C | 20 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0200 others(17): Show |
20 | HG00735.hp2 HG01081.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.775-1907A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579408 | |||||||
| chrX:47579608 | A | G | 2 | a0001c0001t0001g0066 a0001c0001t0001g0139 |
2 | NA18961.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.775-2107T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579608 | |||||||
| chrX:47579614 | A | T | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-2113T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579614 | |||||||
| chrX:47579849 | G | A | 1 | a0001c0001t0001g0152 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.775-2348C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | |||||||
| chrX:47579849 | G | GC | 74 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0057 others(71): Show |
76 | HG00423.hp2 HG00544.hp1 HG00621.hp1 others(73): Show |
intron_variant | MODIFIER | c.775-2349dupG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579849 | |||||||
| chrX:47579863 | C | T | 1 | a0001c0001t0001g0076 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.775-2362G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579863 | |||||||
| chrX:47579879 | G | A | 73 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0057 others(70): Show |
75 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.775-2378C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47579879 | |||||||
| chrX:47580013 | T | G | 1 | a0001c0001t0001g0061 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.775-2512A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580013 | |||||||
| chrX:47580014 | G | T | 1 | a0001c0001t0001g0059 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.775-2513C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580014 | |||||||
| chrX:47580185 | C | CT | 5 | a0001c0001t0001g0059 a0001c0001t0001g0099 a0001c0001t0001g0157 others(2): Show |
5 | HG02895.hp1 HG03942.hp1 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-2685dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580185 | |||||||
| chrX:47580185 | CT | C | 5 | a0001c0001t0001g0054 a0001c0001t0001g0055 a0001c0001t0001g0195 others(2): Show |
5 | HG01496.hp2 HG02896.hp1 NA18987.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-2685delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580185 | |||||||
| chrX:47580201 | T | A | 1 | a0001c0003t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.775-2700A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580201 | |||||||
| chrX:47580248 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.775-2747G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580248 | |||||||
| chrX:47580319 | G | A | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.775-2818C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580319 | |||||||
| chrX:47580341 | T | C | 1 | a0001c0002t0001g0218 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.775-2840A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580341 | |||||||
| chrX:47580354 | G | C | 2 | a0001c0001t0001g0103 a0001c0010t0001g0129 |
2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.775-2853C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580354 | |||||||
| chrX:47580500 | G | A | 1 | a0003c0005t0001g0203 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.775-2999C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580500 | |||||||
| chrX:47580630 | T | TA | 17 | a0001c0001t0001g0045 a0001c0001t0001g0048 a0001c0001t0001g0162 others(14): Show |
17 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.775-3130dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580630 | |||||||
| chrX:47580736 | G | C | 2 | a0001c0002t0001g0041 a0006c0006t0001g0046 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-3235C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580736 | |||||||
| chrX:47580762 | G | C | 80 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(77): Show |
82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.775-3261C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580762 | |||||||
| chrX:47580932 | C | CA | 58 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0050 others(55): Show |
59 | HG00597.hp1 HG00609.hp1 HG00621.hp1 others(56): Show |
intron_variant | MODIFIER | c.775-3432dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47580932 | |||||||
| chrX:47581104 | G | A | 1 | a0001c0001t0001g0196 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.775-3603C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581104 | |||||||
| chrX:47581163 | T | A | 28 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0001g0152 others(25): Show |
31 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.775-3662A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581163 | |||||||
| chrX:47581353 | G | C | 26 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0001g0152 others(23): Show |
29 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.775-3852C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581353 | |||||||
| chrX:47581591 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4090C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581591 | |||||||
| chrX:47581670 | G | A | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.775-4169C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581670 | |||||||
| chrX:47581690 | G | A | 1 | a0001c0002t0001g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.775-4189C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47581690 | |||||||
| chrX:47582062 | G | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG02273.hp2 HG02293.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-4561C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582062 | |||||||
| chrX:47582098 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.775-4597C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582098 | |||||||
| chrX:47582249 | G | A | 1 | a0001c0001t0001g0055 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.775-4748C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582249 | |||||||
| chrX:47582649 | C | A | 16 | a0001c0001t0001g0045 a0001c0001t0001g0162 a0001c0001t0001g0163 others(13): Show |
16 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.775-5148G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47582649 | |||||||
| chrX:47583155 | C | G | 1 | a0001c0001t0001g0116 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.775-5654G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583155 | |||||||
| chrX:47583271 | C | T | 6 | a0001c0001t0001g0004 a0001c0001t0001g0061 a0001c0001t0001g0062 others(3): Show |
8 | NA18960.hp1 NA18971.hp1 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-5770G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583271 | |||||||
| chrX:47583513 | C | T | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.775-6012G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583513 | |||||||
| chrX:47583712 | G | A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(75): Show |
80 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.775-6211C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583712 | |||||||
| chrX:47583841 | G | T | 26 | a0001c0001t0001g0044 a0001c0001t0001g0151 a0001c0001t0001g0152 others(23): Show |
29 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.775-6340C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47583841 | |||||||
| chrX:47584051 | T | C | 2 | a0001c0002t0001g0041 a0006c0006t0001g0046 |
2 | HG03453.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.775-6550A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584051 | |||||||
| chrX:47584106 | G | A | 1 | a0001c0002t0001g0215 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.775-6605C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584106 | |||||||
| chrX:47584130 | G | A | 9 | a0001c0001t0001g0045 a0001c0002t0001g0038 a0001c0002t0001g0042 others(6): Show |
9 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(6): Show |
intron_variant | MODIFIER | c.775-6629C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584130 | |||||||
| chrX:47584207 | G | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0209 a0001c0002t0001g0255 |
3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-6706C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584207 | |||||||
| chrX:47584208 | T | TATTGAGG others(10): Show |
1 | a0001c0003t0002g0214 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.775-6724_775-6708d others(19): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584208 | |||||||
| chrX:47584225 | G | GATTGAGG others(27): Show |
8 | a0001c0001t0001g0146 a0001c0001t0001g0164 a0001c0002t0001g0069 others(5): Show |
8 | HG01243.hp1 HG01346.hp1 HG01884.hp2 others(5): Show |
intron_variant | MODIFIER | c.775-6758_775-6725d others(36): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | |||||||
| chrX:47584225 | G | GATTGAGG others(61): Show |
6 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0166 others(3): Show |
6 | HG02273.hp2 HG02293.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.775-6792_775-6725d others(70): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | |||||||
| chrX:47584225 | G | GATTGAGG others(95): Show |
1 | a0001c0002t0001g0024 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.775-6826_775-6725d others(104): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | |||||||
| chrX:47584225 | G | GATTGAGG others(163): Show |
3 | a0001c0001t0001g0045 a0001c0002t0001g0038 a0001c0002t0001g0042 |
3 | HG02145.hp1 HG02451.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.775-6725_775-6724i others(172): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | |||||||
| chrX:47584225 | GATTGAGG others(27): Show |
G | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.775-6758_775-6725d others(36): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584225 | |||||||
| chrX:47584244 | T | C | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-6743A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584244 | |||||||
| chrX:47584311 | A | G | 2 | a0001c0001t0004g0198 a0001c0003t0002g0212 |
2 | HG00735.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.775-6810T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584311 | |||||||
| chrX:47584392 | T | A | 19 | a0001c0001t0001g0045 a0001c0001t0001g0162 a0001c0001t0001g0163 others(16): Show |
19 | HG00099.hp1 HG01243.hp1 HG01346.hp1 others(16): Show |
intron_variant | MODIFIER | c.775-6891A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584392 | |||||||
| chrX:47584642 | T | G | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.775-7141A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584642 | |||||||
| chrX:47584845 | G | A | 11 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0159 others(8): Show |
11 | HG02258.hp1 HG02559.hp2 HG02630.hp2 others(8): Show |
intron_variant | MODIFIER | c.775-7344C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584845 | |||||||
| chrX:47584857 | T | C | 1 | a0001c0002t0001g0231 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.775-7356A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47584857 | |||||||
| chrX:47585029 | C | T | 1 | a0001c0001t0001g0167 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.775-7528G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585029 | |||||||
| chrX:47585229 | G | C | 1 | a0001c0001t0001g0155 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.775-7728C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585229 | |||||||
| chrX:47585264 | C | T | 1 | a0001c0001t0001g0120 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.775-7763G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585264 | |||||||
| chrX:47585471 | G | A | 1 | a0001c0002t0001g0027 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.775-7970C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585471 | |||||||
| chrX:47585480 | G | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(127): Show |
135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-7979C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585480 | |||||||
| chrX:47585524 | G | A | 6 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(3): Show |
6 | HG02273.hp2 HG02293.hp1 HG03927.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-8023C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585524 | |||||||
| chrX:47585586 | T | C | 130 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(127): Show |
135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-8085A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585586 | |||||||
| chrX:47585767 | T | G | 3 | a0001c0002t0001g0024 a0001c0002t0001g0209 a0001c0002t0001g0255 |
3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-8266A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585767 | |||||||
| chrX:47585824 | C | T | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.775-8323G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585824 | |||||||
| chrX:47585887 | A | G | 130 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(127): Show |
135 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(132): Show |
intron_variant | MODIFIER | c.775-8386T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47585887 | |||||||
| chrX:47586243 | CCT | C | 23 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-8744_775-8743d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586243 | |||||||
| chrX:47586541 | C | T | 23 | a0001c0001t0001g0001 a0001c0001t0001g0006 a0001c0001t0001g0054 others(20): Show |
31 | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(28): Show |
intron_variant | MODIFIER | c.775-9040G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586541 | |||||||
| chrX:47586641 | C | T | 4 | a0001c0001t0001g0091 a0001c0001t0001g0094 a0001c0001t0001g0095 others(1): Show |
4 | NA18948.hp1 NA18968.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-9140G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586641 | |||||||
| chrX:47586696 | T | C | 2 | a0001c0001t0001g0144 a0001c0001t0001g0148 |
2 | HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.775-9195A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586696 | |||||||
| chrX:47586962 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-9461T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47586962 | |||||||
| chrX:47587120 | T | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(125): Show |
133 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-9619A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587120 | |||||||
| chrX:47587254 | G | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(79): Show |
84 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.775-9753C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587254 | |||||||
| chrX:47587258 | G | A | 3 | a0001c0002t0001g0024 a0001c0002t0001g0209 a0001c0002t0001g0255 |
3 | HG02451.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.775-9757C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587258 | |||||||
| chrX:47587737 | C | G | 1 | a0001c0001t0001g0160 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.775-10236G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587737 | |||||||
| chrX:47587760 | C | G | 80 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(77): Show |
82 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.775-10259G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587760 | |||||||
| chrX:47587772 | C | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0209 a0001c0002t0001g0255 others(1): Show |
4 | HG02451.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-10271G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587772 | |||||||
| chrX:47587773 | C | A | 4 | a0001c0002t0001g0024 a0001c0002t0001g0209 a0001c0002t0001g0255 others(1): Show |
4 | HG02451.hp1 HG03486.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.775-10272G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587773 | |||||||
| chrX:47587830 | C | T | 1 | a0001c0002t0001g0022 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.775-10329G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47587830 | |||||||
| chrX:47588199 | G | T | 1 | a0001c0001t0001g0191 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.775-10698C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588199 | |||||||
| chrX:47588359 | A | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-10858T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588359 | |||||||
| chrX:47588428 | C | T | 1 | a0001c0002t0001g0023 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.775-10927G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588428 | |||||||
| chrX:47588476 | C | T | 22 | a0001c0001t0001g0044 a0001c0001t0001g0147 a0001c0001t0001g0162 others(19): Show |
22 | HG00099.hp1 HG01243.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.775-10975G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588476 | |||||||
| chrX:47588486 | G | T | 3 | a0001c0001t0001g0056 a0001c0001t0001g0122 a0001c0001t0001g0125 |
3 | NA18988.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.775-10985C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588486 | |||||||
| chrX:47588525 | C | T | 104 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0050 others(101): Show |
109 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(106): Show |
intron_variant | MODIFIER | c.775-11024G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588525 | |||||||
| chrX:47588605 | C | T | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.775-11104G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588605 | |||||||
| chrX:47588697 | T | C | 128 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(125): Show |
133 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.775-11196A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588697 | |||||||
| chrX:47588714 | T | C | 23 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-11213A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588714 | |||||||
| chrX:47588798 | GGGGTCAC others(8): Show |
G | 2 | a0001c0001t0001g0119 a0001c0001t0001g0124 |
2 | NA18964.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.775-11312_775-1129 others(19): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588798 | |||||||
| chrX:47588876 | G | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0052 others(44): Show |
49 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.775-11375C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588876 | |||||||
| chrX:47588877 | C | A | 47 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0052 others(44): Show |
49 | HG00423.hp2 HG00597.hp1 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.775-11376G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588877 | |||||||
| chrX:47588908 | A | G | 132 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0044 others(129): Show |
139 | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(136): Show |
intron_variant | MODIFIER | c.775-11407T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588908 | |||||||
| chrX:47588939 | G | A | 1 | a0001c0002t0001g0209 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.775-11438C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47588939 | |||||||
| chrX:47589011 | C | T | 75 | a0001c0001t0001g0005 a0001c0001t0001g0050 a0001c0001t0001g0051 others(72): Show |
77 | HG00280.hp1 HG00423.hp2 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.775-11510G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589011 | |||||||
| chrX:47589017 | A | G | 1 | a0001c0002t0001g0032 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.775-11516T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589017 | |||||||
| chrX:47589164 | C | T | 1 | a0001c0001t0001g0107 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.775-11663G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589164 | |||||||
| chrX:47589165 | G | A | 1 | a0002c0004t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.775-11664C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589165 | |||||||
| chrX:47589207 | G | A | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.775-11706C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589207 | |||||||
| chrX:47589258 | C | T | 130 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(127): Show |
148 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.775-11757G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589258 | |||||||
| chrX:47589294 | C | CA | 120 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(117): Show |
138 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.775-11794dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | |||||||
| chrX:47589294 | C | CAA | 7 | a0001c0001t0001g0086 a0001c0001t0001g0109 a0001c0001t0001g0160 others(4): Show |
7 | HG00408.hp1 HG00558.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.775-11795_775-1179 others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | |||||||
| chrX:47589294 | CA | C | 51 | a0001c0001t0001g0044 a0001c0001t0001g0097 a0001c0001t0001g0111 others(48): Show |
54 | HG00099.hp1 HG00735.hp2 HG01243.hp1 others(51): Show |
intron_variant | MODIFIER | c.775-11794delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589294 | |||||||
| chrX:47589311 | A | G | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-11810T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589311 | |||||||
| chrX:47589320 | A | G | 2 | a0001c0001t0001g0081 a0001c0003t0002g0214 |
2 | HG02717.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.775-11819T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589320 | |||||||
| chrX:47589321 | T | C | 5 | a0001c0001t0001g0056 a0001c0001t0001g0081 a0001c0001t0001g0122 others(2): Show |
5 | NA18979.hp2 NA18988.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.775-11820A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589321 | |||||||
| chrX:47589329 | T | C | 8 | a0001c0001t0001g0081 a0001c0001t0001g0110 a0001c0001t0001g0145 others(5): Show |
8 | HG00438.hp1 HG01358.hp1 HG02698.hp1 others(5): Show |
intron_variant | MODIFIER | c.775-11828A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589329 | |||||||
| chrX:47589364 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.775-11863A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589364 | |||||||
| chrX:47589365 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18945.hp1 NA18975.hp2 |
intron_variant | MODIFIER | c.775-11864C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589365 | |||||||
| chrX:47589369 | A | G | 2 | a0001c0002t0002g0011 a0001c0002t0002g0012 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.775-11868T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589369 | |||||||
| chrX:47589389 | C | G | 2 | a0001c0003t0001g0014 a0001c0009t0001g0150 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.775-11888G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589389 | |||||||
| chrX:47589409 | A | C | 4 | a0001c0001t0001g0044 a0001c0001t0001g0163 a0001c0001t0001g0166 others(1): Show |
4 | HG02622.hp2 NA18984.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.775-11908T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589409 | |||||||
| chrX:47589410 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0166 |
2 | NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.775-11909C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589410 | |||||||
| chrX:47589413 | G | A | 2 | a0001c0001t0001g0163 a0001c0001t0001g0166 |
2 | NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.775-11912C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589413 | |||||||
| chrX:47589420 | T | C | 1 | a0001c0001t0001g0176 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11919A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589420 | |||||||
| chrX:47589427 | A | G | 1 | a0001c0001t0001g0176 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11926T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589427 | |||||||
| chrX:47589438 | C | A | 1 | a0001c0001t0001g0176 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.775-11937G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589438 | |||||||
| chrX:47589438 | C | CA | 13 | a0001c0001t0001g0057 a0001c0001t0001g0130 a0001c0001t0001g0156 others(10): Show |
13 | HG01361.hp1 HG02056.hp1 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.775-11938dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589438 | |||||||
| chrX:47589545 | G | A | 29 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0152 others(26): Show |
32 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(29): Show |
intron_variant | MODIFIER | c.775-12044C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589545 | |||||||
| chrX:47589595 | C | CA | 24 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0048 others(21): Show |
25 | HG00621.hp1 HG01346.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.775-12095dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589595 | |||||||
| chrX:47589595 | CA | C | 6 | a0001c0001t0001g0095 a0001c0001t0001g0105 a0001c0001t0001g0106 others(3): Show |
6 | HG01993.hp2 HG03195.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.775-12095delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589595 | |||||||
| chrX:47589760 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12259A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589760 | |||||||
| chrX:47589867 | A | ATAACT | 120 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(117): Show |
125 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.775-12371_775-1236 others(9): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589867 | |||||||
| chrX:47589964 | A | C | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12463T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47589964 | |||||||
| chrX:47590040 | C | G | 1 | a0001c0002t0001g0213 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.775-12539G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590040 | |||||||
| chrX:47590064 | G | A | 2 | a0001c0001t0001g0144 a0001c0001t0001g0148 |
2 | HG02132.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.775-12563C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590064 | |||||||
| chrX:47590173 | C | G | 23 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.775-12672G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590173 | |||||||
| chrX:47590308 | C | G | 1 | a0001c0001t0001g0179 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.775-12807G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590308 | |||||||
| chrX:47590361 | T | A | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.775-12860A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590361 | |||||||
| chrX:47590606 | A | G | 9 | a0001c0001t0001g0047 a0001c0001t0004g0198 a0001c0002t0001g0069 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-13105T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590606 | |||||||
| chrX:47590745 | G | A | 1 | a0002c0004t0001g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.775-13244C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590745 | |||||||
| chrX:47590759 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.775-13258C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590759 | |||||||
| chrX:47590828 | C | T | 20 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(17): Show |
21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.775-13327G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590828 | |||||||
| chrX:47590837 | C | A | 9 | a0001c0001t0001g0047 a0001c0001t0004g0198 a0001c0002t0001g0069 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.775-13336G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590837 | |||||||
| chrX:47590877 | T | C | 86 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(83): Show |
88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.775-13376A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47590877 | |||||||
| chrX:47591165 | G | A | 20 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(17): Show |
21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.775-13664C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591165 | |||||||
| chrX:47591181 | T | C | 111 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(108): Show |
116 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.775-13680A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591181 | |||||||
| chrX:47591442 | C | T | 9 | a0001c0001t0001g0047 a0001c0001t0004g0198 a0001c0002t0001g0069 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+13536G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591442 | |||||||
| chrX:47591550 | G | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(79): Show |
84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+13428C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591550 | |||||||
| chrX:47591720 | C | CA | 31 | a0001c0001t0001g0102 a0001c0001t0001g0152 a0001c0001t0001g0153 others(28): Show |
34 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.774+13257dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591720 | |||||||
| chrX:47591720 | CA | C | 81 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(78): Show |
83 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.774+13257delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591720 | |||||||
| chrX:47591744 | T | C | 3 | a0001c0001t0001g0056 a0001c0001t0001g0122 a0001c0001t0001g0125 |
3 | NA18988.hp1 NA19057.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.774+13234A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591744 | |||||||
| chrX:47591884 | A | G | 1 | a0001c0001t0001g0050 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.774+13094T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47591884 | |||||||
| chrX:47592077 | T | C | 85 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(82): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.774+12901A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592077 | |||||||
| chrX:47592160 | G | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(79): Show |
84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+12818C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592160 | |||||||
| chrX:47592166 | C | T | 1 | a0001c0001t0001g0052 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.774+12812G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592166 | |||||||
| chrX:47592198 | T | A | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+12780A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592198 | |||||||
| chrX:47592337 | C | CAAAT | 17 | a0001c0001t0001g0007 a0001c0001t0001g0184 a0001c0001t0001g0193 others(14): Show |
18 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.774+12637_774+1264 others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592337 | |||||||
| chrX:47592337 | CAAAT | C | 208 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0004 others(205): Show |
227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.774+12637_774+1264 others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592337 | |||||||
| chrX:47592487 | T | C | 1 | a0001c0002t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.774+12491A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592487 | |||||||
| chrX:47592590 | G | A | 23 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+12388C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592590 | |||||||
| chrX:47592987 | G | A | 1 | a0001c0002t0001g0209 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.774+11991C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47592987 | |||||||
| chrX:47593043 | T | C | 22 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(19): Show |
25 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.774+11935A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593043 | |||||||
| chrX:47593048 | G | GT | 23 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+11929dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593048 | |||||||
| chrX:47593147 | G | T | 1 | a0001c0001t0001g0057 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.774+11831C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593147 | |||||||
| chrX:47593183 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.774+11795G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593183 | |||||||
| chrX:47593272 | C | CT | 29 | a0001c0001t0001g0062 a0001c0001t0001g0091 a0001c0001t0001g0145 others(26): Show |
32 | HG01358.hp1 HG01891.hp1 HG01934.hp1 others(29): Show |
intron_variant | MODIFIER | c.774+11705dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593272 | |||||||
| chrX:47593528 | C | G | 9 | a0001c0001t0001g0047 a0001c0001t0004g0198 a0001c0002t0001g0069 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+11450G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593528 | |||||||
| chrX:47593626 | T | C | 4 | a0001c0002t0001g0228 a0001c0002t0001g0231 a0001c0002t0001g0236 others(1): Show |
4 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(1): Show |
intron_variant | MODIFIER | c.774+11352A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593626 | |||||||
| chrX:47593757 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+11221G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47593757 | |||||||
| chrX:47594191 | G | A | 1 | a0001c0001t0001g0115 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.774+10787C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594191 | |||||||
| chrX:47594235 | C | CA | 28 | a0001c0001t0001g0091 a0001c0001t0001g0116 a0001c0001t0001g0152 others(25): Show |
31 | HG01192.hp1 HG01361.hp1 HG01891.hp1 others(28): Show |
intron_variant | MODIFIER | c.774+10742dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594235 | |||||||
| chrX:47594532 | C | CA | 24 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0156 others(21): Show |
27 | HG01891.hp1 HG02056.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.774+10445dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594532 | |||||||
| chrX:47594729 | C | CT | 85 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(82): Show |
87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.774+10248dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594729 | |||||||
| chrX:47594973 | T | A | 3 | a0001c0002t0001g0020 a0001c0002t0001g0209 a0006c0006t0001g0046 |
3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+10005A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47594973 | |||||||
| chrX:47595199 | G | A | 82 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(79): Show |
84 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.774+9779C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595199 | |||||||
| chrX:47595220 | G | T | 3 | a0001c0002t0001g0020 a0001c0002t0001g0209 a0006c0006t0001g0046 |
3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+9758C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595220 | |||||||
| chrX:47595305 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.774+9673G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595305 | |||||||
| chrX:47595396 | T | G | 1 | a0001c0003t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.774+9582A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595396 | |||||||
| chrX:47595643 | A | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0209 a0006c0006t0001g0046 |
3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+9335T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595643 | |||||||
| chrX:47595841 | T | C | 23 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+9137A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595841 | |||||||
| chrX:47595947 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0044 others(125): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.774+9031T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47595947 | |||||||
| chrX:47596054 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8924G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596054 | |||||||
| chrX:47596055 | A | C | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8923T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596055 | |||||||
| chrX:47596057 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8921G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596057 | |||||||
| chrX:47596060 | C | T | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8918G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596060 | |||||||
| chrX:47596061 | C | G | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8917G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596061 | |||||||
| chrX:47596062 | C | A | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8916G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596062 | |||||||
| chrX:47596067 | A | T | 1 | a0001c0001t0001g0174 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.774+8911T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596067 | |||||||
| chrX:47596246 | C | A | 2 | a0001c0002t0002g0011 a0001c0002t0002g0012 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.774+8732G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596246 | |||||||
| chrX:47596392 | G | A | 1 | a0005c0007t0001g0117 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.774+8586C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596392 | |||||||
| chrX:47596418 | A | T | 2 | a0001c0002t0002g0011 a0001c0002t0002g0012 |
2 | HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.774+8560T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596418 | |||||||
| chrX:47596457 | A | G | 1 | a0001c0001t0001g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.774+8521T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596457 | |||||||
| chrX:47596608 | A | G | 1 | a0001c0002t0001g0070 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.774+8370T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596608 | |||||||
| chrX:47596751 | C | T | 136 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0044 others(133): Show |
142 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.774+8227G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596751 | |||||||
| chrX:47596798 | C | T | 7 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(4): Show |
8 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+8180G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596798 | |||||||
| chrX:47596841 | G | A | 2 | a0001c0002t0001g0020 a0006c0006t0001g0046 |
2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.774+8137C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47596841 | |||||||
| chrX:47597243 | G | A | 1 | a0001c0001t0001g0087 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.774+7735C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597243 | |||||||
| chrX:47597296 | T | C | 1 | a0006c0006t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.774+7682A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597296 | |||||||
| chrX:47597335 | C | CA | 14 | a0001c0001t0001g0053 a0001c0001t0001g0157 a0001c0001t0001g0197 others(11): Show |
15 | HG00099.hp1 HG00597.hp2 HG01346.hp1 others(12): Show |
intron_variant | MODIFIER | c.774+7642dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597335 | |||||||
| chrX:47597335 | CA | C | 7 | a0001c0001t0001g0062 a0001c0001t0001g0120 a0001c0001t0001g0135 others(4): Show |
7 | HG01346.hp2 HG01515.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+7642delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597335 | |||||||
| chrX:47597349 | A | G | 21 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(18): Show |
24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+7629T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597349 | |||||||
| chrX:47597502 | G | C | 23 | a0001c0001t0001g0152 a0001c0001t0001g0153 a0001c0001t0001g0184 others(20): Show |
26 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.774+7476C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597502 | |||||||
| chrX:47597518 | C | G | 1 | a0001c0003t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.774+7460G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597518 | |||||||
| chrX:47597554 | G | A | 116 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(113): Show |
121 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.774+7424C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47597554 | |||||||
| chrX:47598044 | G | T | 1 | a0001c0001t0001g0102 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.774+6934C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598044 | |||||||
| chrX:47598098 | G | T | 22 | a0001c0001t0001g0153 a0001c0001t0001g0184 a0001c0001t0001g0187 others(19): Show |
25 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.774+6880C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598098 | |||||||
| chrX:47598223 | AT | A | 7 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(4): Show |
8 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(5): Show |
intron_variant | MODIFIER | c.774+6754delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598223 | |||||||
| chrX:47598400 | GA | G | 49 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(46): Show |
52 | HG00438.hp2 HG01169.hp1 HG01891.hp1 others(49): Show |
intron_variant | MODIFIER | c.774+6577delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598400 | |||||||
| chrX:47598495 | C | T | 2 | a0001c0001t0001g0164 a0001c0001t0001g0165 |
2 | HG03927.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.774+6483G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598495 | |||||||
| chrX:47598514 | A | G | 2 | a0001c0001t0001g0101 a0001c0002t0001g0035 |
2 | HG01074.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.774+6464T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598514 | |||||||
| chrX:47598827 | A | AAAAT | 5 | a0001c0001t0001g0100 a0001c0001t0001g0162 a0001c0001t0001g0163 others(2): Show |
5 | HG02273.hp2 HG02293.hp1 HG02293.hp2 others(2): Show |
intron_variant | MODIFIER | c.774+6147_774+6150d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598827 | |||||||
| chrX:47598841 | A | C | 3 | a0001c0002t0001g0020 a0001c0002t0001g0209 a0006c0006t0001g0046 |
3 | HG02922.hp1 NA19030.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.774+6137T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598841 | |||||||
| chrX:47598904 | C | T | 1 | a0001c0002t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.774+6074G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598904 | |||||||
| chrX:47598925 | G | A | 45 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(42): Show |
48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+6053C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598925 | |||||||
| chrX:47598952 | T | C | 45 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(42): Show |
48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+6026A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598952 | |||||||
| chrX:47598961 | C | T | 1 | a0001c0001t0001g0253 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.774+6017G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47598961 | |||||||
| chrX:47599020 | C | A | 1 | a0001c0002t0001g0026 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.774+5958G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599020 | |||||||
| chrX:47599035 | A | G | 45 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(42): Show |
48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+5943T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599035 | |||||||
| chrX:47599229 | A | G | 1 | a0001c0002t0001g0235 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.774+5749T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599229 | |||||||
| chrX:47599315 | T | C | 137 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0044 others(134): Show |
143 | HG00099.hp1 HG00408.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.774+5663A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599315 | |||||||
| chrX:47599376 | T | C | 1 | a0001c0001t0001g0158 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.774+5602A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599376 | |||||||
| chrX:47599726 | A | G | 128 | a0001c0001t0001g0005 a0001c0001t0001g0007 a0001c0001t0001g0044 others(125): Show |
134 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.774+5252T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599726 | |||||||
| chrX:47599748 | G | A | 1 | a0001c0001t0001g0147 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.774+5230C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47599748 | |||||||
| chrX:47600122 | A | C | 1 | a0001c0001t0001g0128 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.774+4856T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600122 | |||||||
| chrX:47600195 | A | C | 45 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(42): Show |
48 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(45): Show |
intron_variant | MODIFIER | c.774+4783T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600195 | |||||||
| chrX:47600202 | G | GT | 7 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0094 others(4): Show |
7 | HG00733.hp2 HG03927.hp2 HG03942.hp1 others(4): Show |
intron_variant | MODIFIER | c.774+4775dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600202 | |||||||
| chrX:47600446 | G | A | 9 | a0001c0001t0001g0047 a0001c0001t0004g0198 a0001c0002t0001g0069 others(6): Show |
9 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(6): Show |
intron_variant | MODIFIER | c.774+4532C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600446 | |||||||
| chrX:47600474 | G | C | 44 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(41): Show |
47 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+4504C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600474 | |||||||
| chrX:47600526 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.774+4452T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600526 | |||||||
| chrX:47600713 | T | C | 1 | a0001c0002t0001g0216 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.774+4265A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600713 | |||||||
| chrX:47600863 | T | C | 1 | a0001c0001t0001g0118 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.774+4115A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600863 | |||||||
| chrX:47600995 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.774+3983C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47600995 | |||||||
| chrX:47601450 | T | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(17): Show |
21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.774+3528A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601450 | |||||||
| chrX:47601762 | C | G | 43 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(40): Show |
46 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(43): Show |
intron_variant | MODIFIER | c.774+3216G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601762 | |||||||
| chrX:47601893 | A | G | 1 | a0001c0011t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.774+3085T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47601893 | |||||||
| chrX:47602089 | G | A | 3 | a0001c0001t0001g0183 a0001c0001t0001g0185 a0001c0001t0001g0186 |
3 | HG01934.hp1 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.774+2889C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602089 | |||||||
| chrX:47602150 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0052 others(55): Show |
60 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.774+2828G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602150 | |||||||
| chrX:47602388 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.774+2590C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602388 | |||||||
| chrX:47602493 | G | A | 1 | a0001c0002t0001g0072 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.774+2485C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602493 | |||||||
| chrX:47602746 | A | C | 20 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(17): Show |
21 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.774+2232T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602746 | |||||||
| chrX:47602854 | G | C | 44 | a0001c0001t0001g0051 a0001c0001t0001g0055 a0001c0001t0001g0056 others(41): Show |
47 | HG00438.hp2 HG00544.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.774+2124C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47602854 | |||||||
| chrX:47603013 | AT | A | 11 | a0001c0001t0001g0047 a0001c0001t0001g0130 a0001c0001t0001g0177 others(8): Show |
11 | HG00099.hp1 HG00735.hp2 HG01081.hp1 others(8): Show |
intron_variant | MODIFIER | c.774+1964delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603013 | |||||||
| chrX:47603231 | C | T | 58 | a0001c0001t0001g0005 a0001c0001t0001g0045 a0001c0001t0001g0052 others(55): Show |
60 | HG00408.hp2 HG00544.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.774+1747G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603231 | |||||||
| chrX:47603232 | T | G | 105 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(102): Show |
110 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.774+1746A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603232 | |||||||
| chrX:47603397 | A | G | 3 | a0001c0001t0001g0089 a0001c0001t0001g0092 a0001c0001t0001g0093 |
3 | HG01169.hp2 HG03704.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.774+1581T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603397 | |||||||
| chrX:47603457 | AT | A | 3 | a0001c0001t0001g0061 a0001c0001t0001g0140 a0004c0012t0001g0257 |
3 | NA18942.hp1 NA18974.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.774+1520delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603457 | |||||||
| chrX:47603509 | G | C | 79 | a0001c0001t0001g0007 a0001c0001t0001g0044 a0001c0001t0001g0047 others(76): Show |
83 | HG00099.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.774+1469C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603509 | |||||||
| chrX:47603730 | A | C | 1 | a0001c0001t0001g0130 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.774+1248T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603730 | |||||||
| chrX:47603890 | T | TTA | 2 | a0001c0001t0001g0047 a0001c0001t0001g0091 |
2 | HG01081.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.774+1086_774+1087d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603890 | |||||||
| chrX:47603890 | T | TTTTA | 16 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(13): Show |
17 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(14): Show |
intron_variant | MODIFIER | c.774+1087_774+1088i others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603890 | |||||||
| chrX:47603892 | A | T | 2 | a0001c0003t0001g0014 a0001c0009t0001g0150 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.774+1086T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603892 | |||||||
| chrX:47603906 | A | T | 2 | a0001c0001t0001g0064 a0001c0001t0001g0097 |
2 | HG00558.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.774+1072T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | |||||||
| chrX:47603906 | AT | A | 15 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0052 others(12): Show |
16 | HG00597.hp1 HG00621.hp1 HG01123.hp2 others(13): Show |
intron_variant | MODIFIER | c.774+1071delA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603906 | |||||||
| chrX:47603907 | T | TA | 81 | a0001c0001t0001g0045 a0001c0001t0001g0051 a0001c0001t0001g0055 others(78): Show |
82 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(79): Show |
intron_variant | MODIFIER | c.774+1070_774+1071i others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603907 | |||||||
| chrX:47603908 | T | A | 63 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0047 others(60): Show |
68 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.774+1070A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603908 | |||||||
| chrX:47603909 | T | A | 77 | a0001c0001t0001g0005 a0001c0001t0001g0044 a0001c0001t0001g0045 others(74): Show |
79 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(76): Show |
intron_variant | MODIFIER | c.774+1069A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603909 | |||||||
| chrX:47603910 | T | A | 33 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0058 others(30): Show |
34 | HG00099.hp1 HG00735.hp2 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.774+1068A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603910 | |||||||
| chrX:47603911 | T | A | 6 | a0001c0001t0001g0052 a0001c0001t0001g0083 a0001c0001t0001g0142 others(3): Show |
6 | HG00438.hp2 HG00597.hp1 HG01243.hp1 others(3): Show |
intron_variant | MODIFIER | c.774+1067A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603911 | |||||||
| chrX:47603912 | T | A | 25 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0193 others(22): Show |
26 | HG00099.hp1 HG00738.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.774+1066A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603912 | |||||||
| chrX:47603913 | T | A | 2 | a0001c0003t0001g0014 a0001c0009t0001g0150 |
2 | HG01243.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.774+1065A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603913 | |||||||
| chrX:47603914 | T | A | 3 | a0001c0002t0001g0073 a0001c0002t0002g0011 a0001c0002t0002g0012 |
3 | HG02723.hp1 HG02809.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.774+1064A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603914 | |||||||
| chrX:47603938 | G | A | 21 | a0001c0001t0001g0153 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+1040C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47603938 | |||||||
| chrX:47604151 | C | T | 1 | a0001c0002t0001g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.774+827G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604151 | |||||||
| chrX:47604161 | G | A | 21 | a0001c0001t0001g0153 a0001c0001t0001g0184 a0001c0001t0001g0187 others(18): Show |
24 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(21): Show |
intron_variant | MODIFIER | c.774+817C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604161 | |||||||
| chrX:47604168 | C | T | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.774+810G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604168 | |||||||
| chrX:47604179 | G | T | 1 | a0001c0001t0001g0088 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.774+799C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604179 | |||||||
| chrX:47604198 | C | T | 3 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0166 |
3 | HG02273.hp2 NA18984.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.774+780G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604198 | |||||||
| chrX:47604313 | C | T | 19 | a0001c0001t0001g0007 a0001c0001t0001g0047 a0001c0001t0001g0097 others(16): Show |
20 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(17): Show |
intron_variant | MODIFIER | c.774+665G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604313 | |||||||
| chrX:47604345 | C | T | 1 | a0001c0002t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.774+633G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604345 | |||||||
| chrX:47604441 | C | T | 18 | a0001c0001t0001g0007 a0001c0001t0001g0193 a0001c0001t0001g0194 others(15): Show |
19 | HG00738.hp1 HG00741.hp2 HG01070.hp1 others(16): Show |
intron_variant | MODIFIER | c.774+537G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604441 | |||||||
| chrX:47604488 | T | C | 1 | a0002c0004t0001g0258 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.774+490A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604488 | |||||||
| chrX:47604892 | GC | G | 74 | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0080 others(71): Show |
75 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.774+85delG | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 5/12 | chrX | 47604892 | |||||||
| chrX:47605398 | G | A | 1 | a0001c0003t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.528-19C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605398 | |||||||
| chrX:47605713 | C | A | 4 | a0001c0001t0001g0044 a0001c0002t0001g0015 a0001c0002t0002g0011 others(1): Show |
4 | HG01891.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.528-334G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605713 | |||||||
| chrX:47605893 | A | T | 20 | a0001c0001t0001g0059 a0001c0001t0001g0060 a0001c0001t0001g0061 others(17): Show |
20 | HG00423.hp2 HG00544.hp2 HG00733.hp1 others(17): Show |
intron_variant | MODIFIER | c.528-514T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605893 | |||||||
| chrX:47605908 | T | C | 3 | a0001c0002t0001g0015 a0001c0002t0002g0011 a0001c0002t0002g0012 |
3 | HG01891.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.528-529A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605908 | |||||||
| chrX:47605923 | C | T | 1 | a0001c0001t0001g0049 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.528-544G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605923 | |||||||
| chrX:47605927 | C | G | 3 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0042 |
3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.528-548G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605927 | |||||||
| chrX:47605948 | G | A | 1 | a0001c0002t0001g0209 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.528-569C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605948 | |||||||
| chrX:47605971 | T | C | 3 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0042 |
3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.528-592A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47605971 | |||||||
| chrX:47606247 | G | A | 1 | a0001c0011t0001g0243 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.527+698C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606247 | |||||||
| chrX:47606295 | C | CT | 82 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(79): Show |
86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.527+649dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606295 | |||||||
| chrX:47606296 | T | C | 3 | a0001c0002t0001g0038 a0001c0002t0001g0039 a0001c0002t0001g0042 |
3 | HG02145.hp1 HG03195.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.527+649A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606296 | |||||||
| chrX:47606730 | A | AAT | 7 | a0001c0001t0001g0151 a0001c0001t0001g0152 a0001c0001t0001g0153 others(4): Show |
7 | HG01243.hp1 HG02559.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.527+213_527+214dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606730 | |||||||
| chrX:47606747 | A | T | 2 | a0001c0002t0001g0018 a0001c0002t0001g0037 |
2 | HG00738.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.527+198T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606747 | |||||||
| chrX:47606749 | A | AT | 5 | a0001c0002t0001g0017 a0001c0002t0001g0019 a0001c0002t0001g0027 others(2): Show |
5 | HG02055.hp1 HG02723.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.527+195dupA | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606749 | |||||||
| chrX:47606749 | A | T | 18 | a0001c0002t0001g0016 a0001c0002t0001g0018 a0001c0002t0001g0020 others(15): Show |
18 | HG00408.hp1 HG00544.hp1 HG00738.hp1 others(15): Show |
intron_variant | MODIFIER | c.527+196T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606749 | |||||||
| chrX:47606751 | A | T | 82 | a0001c0001t0001g0050 a0001c0001t0001g0057 a0001c0001t0001g0076 others(79): Show |
86 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.527+194T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606751 | |||||||
| chrX:47606753 | T | A | 6 | a0001c0001t0001g0045 a0001c0001t0001g0125 a0001c0001t0001g0130 others(3): Show |
6 | HG02451.hp2 HG02622.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.527+192A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606753 | |||||||
| chrX:47606794 | C | T | 1 | a0001c0002t0001g0249 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.527+151G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 3/12 | chrX | 47606794 | |||||||
| chrX:47607114 | C | G | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.435+27G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 2/12 | chrX | 47607114 | |||||||
| chrX:47607217 | A | T | 1 | a0001c0002t0001g0030 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.378-19T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607217 | |||||||
| chrX:47607244 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.378-46C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607244 | |||||||
| chrX:47607479 | T | C | 94 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0002t0001g0003 others(91): Show |
98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-281A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607479 | |||||||
| chrX:47607519 | C | T | 94 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0002t0001g0003 others(91): Show |
98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-321G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607519 | |||||||
| chrX:47607521 | C | T | 3 | a0001c0001t0001g0047 a0002c0004t0001g0258 a0002c0004t0001g0259 |
3 | HG01081.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.378-323G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607521 | |||||||
| chrX:47607551 | C | T | 10 | a0001c0002t0001g0003 a0001c0002t0001g0022 a0001c0002t0001g0023 others(7): Show |
13 | HG01891.hp1 HG02109.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.378-353G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607551 | |||||||
| chrX:47607560 | C | T | 6 | a0001c0002t0001g0015 a0001c0002t0001g0038 a0001c0002t0001g0039 others(3): Show |
6 | HG01891.hp2 HG02145.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-362G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607560 | |||||||
| chrX:47607616 | G | A | 24 | a0001c0002t0001g0003 a0001c0002t0001g0022 a0001c0002t0001g0023 others(21): Show |
27 | HG00099.hp1 HG00735.hp2 HG01346.hp1 others(24): Show |
intron_variant | MODIFIER | c.378-418C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607616 | |||||||
| chrX:47607727 | G | GA | 18 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0001t0001g0079 others(15): Show |
18 | HG00408.hp2 HG00642.hp1 HG01081.hp1 others(15): Show |
intron_variant | MODIFIER | c.378-530dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | |||||||
| chrX:47607727 | G | GAA | 73 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0015 others(70): Show |
77 | HG00099.hp1 HG00408.hp1 HG00609.hp1 others(74): Show |
intron_variant | MODIFIER | c.378-531_378-530dup others(2): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | |||||||
| chrX:47607727 | G | GAAA | 9 | a0001c0002t0001g0017 a0001c0002t0001g0036 a0001c0002t0001g0211 others(6): Show |
9 | HG00544.hp1 HG01516.hp1 HG01891.hp1 others(6): Show |
intron_variant | MODIFIER | c.378-532_378-530dup others(3): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607727 | |||||||
| chrX:47607746 | C | A | 4 | a0001c0001t0001g0057 a0001c0001t0001g0130 a0001c0003t0002g0212 others(1): Show |
4 | HG00735.hp2 NA18942.hp1 NA19063.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-548G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607746 | |||||||
| chrX:47607757 | G | A | 1 | a0006c0006t0001g0046 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.378-559C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47607757 | |||||||
| chrX:47608001 | G | A | 84 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(81): Show |
88 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.378-803C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608001 | |||||||
| chrX:47608245 | AGGAAGGA others(39): Show |
A | 1 | a0001c0002t0001g0250 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.378-1093_378-1048d others(48): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608245 | |||||||
| chrX:47608259 | GAAGGAAG others(19): Show |
G | 6 | a0001c0002t0001g0034 a0001c0002t0001g0043 a0001c0002t0001g0228 others(3): Show |
6 | HG00741.hp1 HG01433.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.378-1087_378-1062d others(28): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608259 | |||||||
| chrX:47608263 | GAAGGAAG others(15): Show |
G | 38 | a0001c0002t0001g0018 a0001c0002t0001g0020 a0001c0002t0001g0021 others(35): Show |
38 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(35): Show |
intron_variant | MODIFIER | c.378-1087_378-1066d others(24): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608263 | |||||||
| chrX:47608267 | GAAGGAAG others(11): Show |
G | 31 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(28): Show |
35 | HG01346.hp1 HG01361.hp1 HG01891.hp1 others(32): Show |
intron_variant | MODIFIER | c.378-1087_378-1070d others(20): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608267 | |||||||
| chrX:47608271 | GAAGGAAG others(7): Show |
G | 7 | a0001c0001t0001g0044 a0001c0002t0001g0017 a0001c0002t0001g0023 others(4): Show |
7 | HG00099.hp1 HG01884.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1087_378-1074d others(16): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608271 | |||||||
| chrX:47608275 | GAAGGAAG others(3): Show |
G | 3 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0002g0212 |
3 | HG00735.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.378-1087_378-1078d others(12): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608275 | |||||||
| chrX:47608279 | GAAGGAA | G | 8 | a0001c0001t0001g0008 a0001c0001t0001g0090 a0001c0001t0001g0126 others(5): Show |
8 | HG00642.hp1 HG01081.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-1087_378-1082d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608279 | |||||||
| chrX:47608283 | G | A | 2 | a0001c0001t0001g0103 a0001c0010t0001g0129 |
2 | NA18990.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.378-1085C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608283 | |||||||
| chrX:47608283 | GAA | G | 13 | a0001c0001t0001g0008 a0001c0001t0001g0047 a0001c0001t0001g0184 others(10): Show |
13 | HG01081.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.378-1087_378-1086d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608283 | |||||||
| chrX:47608288 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0137 others(6): Show |
10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1090T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608288 | |||||||
| chrX:47608289 | A | G | 9 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0137 others(6): Show |
10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1091T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608289 | |||||||
| chrX:47608289 | AGG | A | 105 | a0001c0001t0001g0008 a0001c0001t0001g0044 a0001c0001t0001g0047 others(102): Show |
110 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.378-1093_378-1092d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608289 | |||||||
| chrX:47608290 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0137 others(6): Show |
10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1092C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608290 | |||||||
| chrX:47608291 | G | A | 9 | a0001c0001t0001g0007 a0001c0001t0001g0045 a0001c0001t0001g0137 others(6): Show |
10 | HG00741.hp2 HG01070.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.378-1093C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGAAG others(21): Show |
1 | a0001c0001t0001g0158 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.378-1094_378-1093i others(30): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGAAG others(17): Show |
4 | a0001c0001t0001g0053 a0001c0001t0001g0113 a0001c0001t0001g0124 others(1): Show |
4 | HG00597.hp2 NA18964.hp2 NA19081.hp2 others(1): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(26): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGAAG others(13): Show |
13 | a0001c0001t0001g0004 a0001c0001t0001g0078 a0001c0001t0001g0093 others(10): Show |
15 | HG00280.hp1 HG00558.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(22): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGAAG others(9): Show |
35 | a0001c0001t0001g0002 a0001c0001t0001g0055 a0001c0001t0001g0076 others(32): Show |
39 | HG00735.hp1 HG01099.hp1 HG01106.hp1 others(36): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(18): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGAAG others(5): Show |
34 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0058 others(31): Show |
37 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(34): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GAAGGGGA others(1): Show |
39 | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0005 others(36): Show |
40 | HG00140.hp1 HG00423.hp1 HG00558.hp1 others(37): Show |
intron_variant | MODIFIER | c.378-1094_378-1093i others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608291 | G | GGGAA | 19 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0013 others(16): Show |
21 | HG01070.hp2 HG01167.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.378-1097_378-1094d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608291 | |||||||
| chrX:47608507 | G | C | 3 | a0001c0002t0001g0015 a0001c0002t0002g0011 a0001c0002t0002g0012 |
3 | HG01891.hp2 HG02723.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.378-1309C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608507 | |||||||
| chrX:47608673 | C | T | 1 | a0001c0001t0001g0080 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.378-1475G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608673 | |||||||
| chrX:47608863 | A | G | 94 | a0001c0001t0001g0044 a0001c0001t0001g0047 a0001c0002t0001g0003 others(91): Show |
98 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(95): Show |
intron_variant | MODIFIER | c.378-1665T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608863 | |||||||
| chrX:47608886 | G | GAC | 63 | a0001c0001t0001g0007 a0001c0001t0001g0013 a0001c0001t0001g0132 others(60): Show |
67 | HG00408.hp1 HG00544.hp1 HG00733.hp2 others(64): Show |
intron_variant | MODIFIER | c.378-1690_378-1689d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | |||||||
| chrX:47608886 | G | GACAC | 47 | a0001c0001t0001g0008 a0001c0001t0001g0142 a0001c0001t0001g0190 others(44): Show |
49 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.378-1692_378-1689d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | |||||||
| chrX:47608886 | GAC | G | 10 | a0001c0001t0001g0044 a0001c0001t0001g0050 a0001c0001t0001g0053 others(7): Show |
10 | HG00597.hp2 HG01243.hp1 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1690_378-1689d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | |||||||
| chrX:47608886 | GACAC | G | 6 | a0001c0001t0001g0047 a0001c0001t0001g0077 a0001c0001t0001g0078 others(3): Show |
6 | HG01081.hp1 HG02015.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.378-1692_378-1689d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608886 | |||||||
| chrX:47608935 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.378-1737G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47608935 | |||||||
| chrX:47609005 | G | C | 1 | a0002c0004t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378-1807C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GAC | 14 | a0001c0001t0001g0048 a0001c0001t0001g0064 a0001c0001t0001g0143 others(11): Show |
14 | HG00558.hp1 HG01358.hp1 HG02132.hp1 others(11): Show |
intron_variant | MODIFIER | c.378-1809_378-1808d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACAC | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0013 others(48): Show |
53 | HG00280.hp1 HG00741.hp2 HG01070.hp1 others(50): Show |
intron_variant | MODIFIER | c.378-1811_378-1808d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACAC | 37 | a0001c0001t0001g0167 a0001c0001t0001g0200 a0001c0002t0001g0009 others(34): Show |
38 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.378-1813_378-1808d others(8): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(1): Show |
17 | a0001c0002t0001g0018 a0001c0002t0001g0021 a0001c0002t0001g0030 others(14): Show |
17 | HG00544.hp1 HG00738.hp1 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.378-1815_378-1808d others(10): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(3): Show |
11 | a0001c0002t0001g0003 a0001c0002t0001g0022 a0001c0002t0001g0023 others(8): Show |
14 | HG01891.hp1 HG02109.hp2 HG02257.hp1 others(11): Show |
intron_variant | MODIFIER | c.378-1817_378-1808d others(12): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(5): Show |
7 | a0001c0002t0001g0041 a0001c0002t0001g0070 a0001c0002t0001g0071 others(4): Show |
7 | HG00099.hp1 HG02630.hp2 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.378-1819_378-1808d others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(7): Show |
1 | a0001c0002t0001g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378-1821_378-1808d others(16): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(9): Show |
1 | a0001c0002t0001g0037 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.378-1823_378-1808d others(18): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | G | GACACACA others(11): Show |
1 | a0001c0002t0001g0073 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.378-1825_378-1808d others(20): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | GAC | G | 9 | a0001c0001t0001g0005 a0001c0001t0001g0052 a0001c0001t0001g0058 others(6): Show |
10 | HG00597.hp1 HG00621.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.378-1809_378-1808d others(4): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609005 | GACAC | G | 4 | a0001c0001t0001g0076 a0001c0002t0001g0038 a0001c0002t0001g0039 others(1): Show |
4 | HG01123.hp2 HG02145.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-1811_378-1808d others(6): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609005 | |||||||
| chrX:47609131 | G | A | 82 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(79): Show |
86 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.378-1933C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609131 | |||||||
| chrX:47609343 | T | C | 59 | a0001c0002t0001g0009 a0001c0002t0001g0016 a0001c0002t0001g0017 others(56): Show |
60 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.378-2145A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609343 | |||||||
| chrX:47609345 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0001g0161 |
2 | HG00558.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.378-2147A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609345 | |||||||
| chrX:47609432 | C | T | 81 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(78): Show |
85 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.378-2234G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609432 | |||||||
| chrX:47609575 | C | T | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-2377G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609575 | |||||||
| chrX:47609889 | G | A | 1 | a0001c0001t0001g0058 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.378-2691C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47609889 | |||||||
| chrX:47610034 | G | A | 8 | a0001c0001t0001g0162 a0001c0001t0001g0163 a0001c0001t0001g0164 others(5): Show |
8 | HG02074.hp1 HG02273.hp2 HG02293.hp1 others(5): Show |
intron_variant | MODIFIER | c.378-2836C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610034 | |||||||
| chrX:47610199 | C | T | 1 | a0001c0002t0001g0021 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.378-3001G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610199 | |||||||
| chrX:47610200 | G | A | 1 | a0001c0001t0001g0168 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.378-3002C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610200 | |||||||
| chrX:47610420 | T | C | 1 | a0001c0002t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.378-3222A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610420 | |||||||
| chrX:47610501 | G | A | 1 | a0002c0004t0001g0259 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.378-3303C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610501 | |||||||
| chrX:47610739 | T | C | 4 | a0001c0002t0001g0015 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3541A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610739 | |||||||
| chrX:47610953 | A | G | 1 | a0001c0002t0003g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.378-3755T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610953 | |||||||
| chrX:47610958 | C | T | 4 | a0001c0002t0001g0015 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3760G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610958 | |||||||
| chrX:47610959 | G | T | 3 | a0001c0001t0001g0065 a0001c0001t0001g0066 a0001c0001t0001g0067 |
3 | NA18961.hp1 NA18970.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.378-3761C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47610959 | |||||||
| chrX:47611047 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-3849T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611047 | |||||||
| chrX:47611084 | A | G | 4 | a0001c0002t0002g0011 a0001c0002t0002g0012 a0001c0003t0001g0014 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-3886T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611084 | |||||||
| chrX:47611181 | A | G | 1 | a0001c0001t0001g0064 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.378-3983T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611181 | |||||||
| chrX:47611326 | A | G | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-4128T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611326 | |||||||
| chrX:47611430 | C | T | 87 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(84): Show |
91 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.378-4232G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611430 | |||||||
| chrX:47611577 | G | T | 76 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.378-4379C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611577 | |||||||
| chrX:47611859 | CCAAAGAA others(5): Show |
C | 76 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.378-4673_378-4662d others(14): Show |
SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611859 | |||||||
| chrX:47611916 | A | C | 1 | a0001c0003t0002g0212 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.378-4718T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611916 | |||||||
| chrX:47611961 | A | C | 1 | a0001c0001t0001g0063 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.378-4763T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47611961 | |||||||
| chrX:47612228 | G | C | 1 | a0001c0002t0001g0222 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.378-5030C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612228 | |||||||
| chrX:47612232 | T | C | 4 | a0001c0001t0001g0044 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.378-5034A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612232 | |||||||
| chrX:47612538 | T | G | 88 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(85): Show |
92 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.378-5340A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612538 | |||||||
| chrX:47612557 | G | A | 1 | a0001c0001t0001g0169 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.378-5359C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612557 | |||||||
| chrX:47612678 | G | T | 3 | a0001c0001t0001g0060 a0001c0001t0001g0061 a0001c0001t0001g0062 |
3 | NA18952.hp1 NA18974.hp1 NA18992.hp2 |
intron_variant | MODIFIER | c.378-5480C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612678 | |||||||
| chrX:47612804 | C | A | 1 | a0001c0001t0001g0170 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.378-5606G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612804 | |||||||
| chrX:47612819 | A | T | 11 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(8): Show |
11 | HG01081.hp1 HG01884.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.378-5621T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612819 | |||||||
| chrX:47612899 | G | A | 3 | a0001c0001t0001g0059 a0001c0001t0001g0171 a0001c0001t0001g0172 |
3 | NA19060.hp1 NA19070.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.378-5701C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612899 | |||||||
| chrX:47612902 | G | A | 1 | a0001c0002t0003g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.378-5704C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612902 | |||||||
| chrX:47612990 | G | A | 1 | a0001c0001t0001g0173 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.378-5792C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47612990 | |||||||
| chrX:47613005 | C | T | 1 | a0001c0002t0001g0020 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.378-5807G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613005 | |||||||
| chrX:47613131 | C | CA | 12 | a0001c0001t0001g0051 a0001c0001t0001g0174 a0001c0001t0001g0175 others(9): Show |
12 | HG00735.hp1 HG01884.hp2 HG02071.hp1 others(9): Show |
intron_variant | MODIFIER | c.378-5934dupT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | |||||||
| chrX:47613131 | CA | C | 82 | a0001c0001t0001g0005 a0001c0001t0001g0013 a0001c0001t0001g0050 others(79): Show |
87 | HG00408.hp2 HG00544.hp1 HG00597.hp1 others(84): Show |
intron_variant | MODIFIER | c.378-5934delT | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613131 | |||||||
| chrX:47613156 | A | G | 1 | a0001c0001t0001g0045 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.378-5958T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613156 | |||||||
| chrX:47613181 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.378-5983C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613181 | |||||||
| chrX:47613332 | T | C | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.377+6020A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613332 | |||||||
| chrX:47613615 | C | T | 4 | a0001c0001t0001g0044 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5737G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613615 | |||||||
| chrX:47613736 | C | T | 76 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+5616G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613736 | |||||||
| chrX:47613738 | C | A | 1 | a0001c0001t0001g0206 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.377+5614G>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613738 | |||||||
| chrX:47613766 | T | C | 88 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0047 others(85): Show |
92 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.377+5586A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613766 | |||||||
| chrX:47613833 | A | G | 9 | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(6): Show |
9 | HG01934.hp1 HG02258.hp1 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.377+5519T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613833 | |||||||
| chrX:47613875 | G | A | 3 | a0001c0001t0001g0047 a0002c0004t0001g0258 a0002c0004t0001g0259 |
3 | HG01081.hp1 HG03516.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.377+5477C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613875 | |||||||
| chrX:47613914 | C | T | 1 | a0001c0002t0001g0019 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.377+5438G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613914 | |||||||
| chrX:47613916 | G | T | 3 | a0001c0002t0001g0009 a0001c0002t0001g0244 a0001c0002t0001g0245 |
4 | NA18953.hp1 NA19000.hp1 NA19009.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5436C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47613916 | |||||||
| chrX:47614182 | C | T | 4 | a0001c0001t0001g0044 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG02622.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+5170G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614182 | |||||||
| chrX:47614377 | G | C | 1 | a0001c0002t0001g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.377+4975C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614377 | |||||||
| chrX:47614497 | T | C | 62 | a0001c0001t0001g0050 a0001c0002t0001g0009 a0001c0002t0001g0016 others(59): Show |
63 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.377+4855A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614497 | |||||||
| chrX:47614572 | C | G | 76 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+4780G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614572 | |||||||
| chrX:47614715 | C | G | 2 | a0001c0002t0001g0210 a0001c0002t0001g0211 |
2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.377+4637G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614715 | |||||||
| chrX:47614777 | C | T | 76 | a0001c0002t0001g0003 a0001c0002t0001g0009 a0001c0002t0001g0016 others(73): Show |
80 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(77): Show |
intron_variant | MODIFIER | c.377+4575G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47614777 | |||||||
| chrX:47615243 | A | T | 1 | a0001c0002t0001g0018 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.377+4109T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615243 | |||||||
| chrX:47615430 | C | T | 1 | a0001c0001t0001g0051 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.377+3922G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47615430 | |||||||
| chrX:47616051 | C | G | 92 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0045 others(89): Show |
96 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(93): Show |
intron_variant | MODIFIER | c.377+3301G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616051 | |||||||
| chrX:47616210 | C | G | 1 | a0001c0002t0001g0209 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.377+3142G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616210 | |||||||
| chrX:47616372 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2980T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616372 | |||||||
| chrX:47616373 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2979T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616373 | |||||||
| chrX:47616374 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2978T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616374 | |||||||
| chrX:47616375 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2977C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616375 | |||||||
| chrX:47616376 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2976T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616376 | |||||||
| chrX:47616379 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2973T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616379 | |||||||
| chrX:47616386 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2966T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616386 | |||||||
| chrX:47616391 | T | A | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2961A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616391 | |||||||
| chrX:47616392 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2960A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616392 | |||||||
| chrX:47616394 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2958T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616394 | |||||||
| chrX:47616400 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2952A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616400 | |||||||
| chrX:47616403 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2949A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616403 | |||||||
| chrX:47616404 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2948A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616404 | |||||||
| chrX:47616406 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2946A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616406 | |||||||
| chrX:47616408 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2944C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616408 | |||||||
| chrX:47616413 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2939C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616413 | |||||||
| chrX:47616419 | G | A | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2933C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616419 | |||||||
| chrX:47616425 | G | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2927C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616425 | |||||||
| chrX:47616428 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2924T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616428 | |||||||
| chrX:47616429 | G | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2923C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616429 | |||||||
| chrX:47616431 | A | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2921T>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616431 | |||||||
| chrX:47616432 | T | C | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2920A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616432 | |||||||
| chrX:47616436 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2916T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616436 | |||||||
| chrX:47616438 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2914T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616438 | |||||||
| chrX:47616440 | A | T | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2912T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616440 | |||||||
| chrX:47616442 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2910T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616442 | |||||||
| chrX:47616444 | T | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2908A>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616444 | |||||||
| chrX:47616446 | A | G | 1 | a0001c0001t0001g0048 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.377+2906T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616446 | |||||||
| chrX:47616665 | A | G | 1 | a0001c0002t0001g0015 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.377+2687T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616665 | |||||||
| chrX:47616973 | T | C | 1 | a0001c0001t0001g0181 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.377+2379A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47616973 | |||||||
| chrX:47617051 | A | G | 2 | a0001c0002t0001g0016 a0001c0002t0001g0017 |
2 | HG02055.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.377+2301T>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617051 | |||||||
| chrX:47617414 | T | A | 1 | a0001c0002t0001g0043 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.377+1938A>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617414 | |||||||
| chrX:47617513 | G | T | 78 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0002t0001g0003 others(75): Show |
82 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(79): Show |
intron_variant | MODIFIER | c.377+1839C>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617513 | |||||||
| chrX:47617842 | G | A | 1 | a0001c0002t0003g0010 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.377+1510C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617842 | |||||||
| chrX:47617860 | G | C | 25 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0183 others(22): Show |
27 | HG00741.hp2 HG01070.hp1 HG01167.hp1 others(24): Show |
intron_variant | MODIFIER | c.377+1492C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617860 | |||||||
| chrX:47617878 | A | T | 4 | a0001c0002t0001g0015 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG01891.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+1474T>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617878 | |||||||
| chrX:47617966 | G | C | 1 | a0001c0003t0001g0014 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.377+1386C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47617966 | |||||||
| chrX:47618022 | T | C | 13 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0002t0001g0009 others(10): Show |
14 | HG00408.hp2 HG00609.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.377+1330A>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618022 | |||||||
| chrX:47618068 | C | T | 90 | a0001c0001t0001g0013 a0001c0001t0001g0044 a0001c0001t0001g0045 others(87): Show |
94 | HG00408.hp2 HG00544.hp1 HG00609.hp1 others(91): Show |
intron_variant | MODIFIER | c.377+1284G>A | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618068 | |||||||
| chrX:47618269 | G | C | 3 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0002t0001g0204 |
3 | NA18945.hp1 NA18975.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.377+1083C>G | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618269 | |||||||
| chrX:47618690 | C | G | 4 | a0001c0001t0001g0013 a0001c0002t0002g0011 a0001c0002t0002g0012 others(1): Show |
4 | HG01884.hp2 HG02723.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.377+662G>C | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618690 | |||||||
| chrX:47618702 | G | A | 2 | a0001c0001t0001g0207 a0001c0001t0001g0208 |
2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.377+650C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618702 | |||||||
| chrX:47618786 | G | A | 50 | a0001c0001t0001g0253 a0001c0001t0001g0254 a0001c0002t0001g0003 others(47): Show |
54 | HG00408.hp2 HG00609.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.377+566C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47618786 | |||||||
| chrX:47619178 | G | A | 1 | a0001c0002t0001g0255 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.377+174C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47619178 | |||||||
| chrX:47619273 | G | A | 1 | a0001c0002t0001g0256 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.377+79C>T | SYN1 | ENSG00000008056.14 | transcript | ENST00000295987.13 | protein_coding | 1/12 | chrX | 47619273 |